0,1,2,3,4,5,correct,choiceA_probs,choiceB_probs,choiceC_probs,choiceD_probs
In a Robertsonian translocation fusion occurs at the:,telomeres.,centromeres.,histones.,ends of the long arms.,B,True,0.10049746930599213,0.1656923145055771,0.10049746930599213,0.12904131412506104
Zinc finger proteins and helix-turn-helix proteins are,types of DNA-binding proteins,involved in the control of translation,components of ribosomes,part of the hemoglobin in blood cells,A,True,0.26232481002807617,0.0851643979549408,0.0663260966539383,0.10935324430465698
"If the frequency of males affected with an X-linked recessive condition in a human population is .10 (one in ten), what will be the expected frequency of affected females?",0.01,0.001,0.02,0.0001,A,False,0.10736805945634842,0.15621960163116455,0.13786330819129944,0.22729817032814026
In DNA adenine normally pairs with:,cytosine.,guanine.,thymine.,uracil.,C,False,0.29288432002067566,0.1220923438668251,0.09508561342954636,0.10774613171815872
The pattern of inheritance shown by malignant hyperthermia (hyperpyrexia) is:,autosomal dominant.,autosomal recessive.,X-linked dominant.,X-linked recessive.,A,True,0.19991958141326904,0.1764284074306488,0.10700924694538116,0.12125736474990845
Mapping of human chromosomes:,has been restricted to the sex chromosomes because of small family sizes,proceeded much more successfully as large numbers of DNA markers became available.,has determined that the number of linkage groups is about twice the number of chromosomes,has demonstrated that almost all of the DNA is involved in coding for genes,B,False,0.16829828917980194,0.16829828917980194,0.09008358418941498,0.14852271974086761
Intergenerational transmission to offspring can occur as a result of parental exposures to ______.,war,natural disasters,hunger,all of these,D,True,0.0429447703063488,0.04866279661655426,0.0624842643737793,0.3173213005065918
Asp235Phe in a molecular report indicates that:,asparagine has been replaced by phenylalanine.,phenylalanine has been replaced by asparagine.,aspartic acid has been replaced by phenylalanine.,phenylalanine has been replaced by aspartic acid.,C,False,0.1797412633895874,0.12353423237800598,0.0849037617444992,0.12353423237800598
The risk of abnormality in the child of a mother with untreated phenylketonuria is:,1%,10%,25%,Almost 100%,D,False,0.20508894324302673,0.14095543324947357,0.12439273297786713,0.14095543324947357
Exon skipping is associated with:,nonsense mutations.,regulatory mutations.,RNA processing mutations.,silent mutations.,C,False,0.14505815505981445,0.12801337242126465,0.14505815505981445,0.14505815505981445
Which of the following is not a chromosome instability syndrome?,Klinefelter syndrome,Ataxia telangiectasia,Fanconi anaemia,Bloom syndrome,A,False,0.14429782330989838,0.09917435050010681,0.1273423731327057,0.20995208621025085
Normal adult haemoglobin (Hb A) consists of:,two α (alpha) and two β (beta) chains.,two α and two γ (gamma) chains.,two α and two δ (delta) chains.,four γ chains.,A,True,0.2515698969364166,0.09254739433526993,0.056132830679416656,0.15258486568927765
In a condition such as schizophrenia the recurrence risk will be greatest for which of the following relatives of an affected individual?,Brother,Nephew,Grandchild,Aunt,A,True,0.17578144371509552,0.09408903121948242,0.15512658655643463,0.12081269919872284
The mutation in sickle-cell disease consists of:,a deletion.,a duplication.,an insertion.,a point mutation.,D,False,0.21093177795410156,0.1129036471247673,0.1129036471247673,0.16427382826805115
Which of the following is an example of monosomy?,"46,XX","47,XXX","69,XYY","45,X",D,True,0.16195614635944366,0.1261315792798996,0.11131072789430618,0.1835203617811203
QTL analysis is used to,identify chromosome regions associated with a complex trait in a genetic cross,determine which genes are expressed at a developmental stage,map genes in bacterial viruses,identify RNA polymerase binding sites,A,True,0.2950195372104645,0.07459262013435364,0.09577882289886475,0.1229824349284172
What would be the frequency of AABBCC individuals from a mating of two AaBbCc individuals?,1.0/64,1.0/32,1.0/128,1.0/256,A,True,0.2034228891134262,0.08479927480220795,0.12338221818208694,0.17952005565166473
It is currently estimated that there are ______ human protein-coding genes although this estimate may be reduced over time.,"10,000–15,000","19,000–20,000","29,000–30,000","100,000",B,False,0.27746981382369995,0.10207545012235641,0.07949642837047577,0.11566662043333054
With which of the following relatives is an individual most likely to share a common HLA haplotype?,Father,Mother,Sister,Son,C,False,0.14192937314510345,0.0975465402007103,0.12525224685668945,0.12525224685668945
Which of the following genes conveys susceptibility for polygenic Alzheimer disease?,APP,PS1,PS2,APOE,D,True,0.1745077222585678,0.07274563610553741,0.09340725094079971,0.19774314761161804
The DiGeorge/Shprintzen syndrome is caused by a deletion in which chromosome?,4,7,15,22,D,True,0.10764530301094055,0.13821931183338165,0.1566230058670044,0.201107919216156
X-chromosome inactivation,results in genetically turning off one of the two X chromosomes in female mammals,takes place in humans so that the same X chromosome is inactive in all of the cells of a female,is the cause of the Y chromosome being genetically inactive,occurs in fruit flies but not in mammals,A,True,0.2929669916629791,0.09511245787143707,0.06536976248025894,0.10777653008699417
The pattern of inheritance shown by glucose-6-phosphate dehydrogenase (G6PD) deficiency is:,autosomal dominant.,autosomal recessive.,X-linked dominant.,X-linked recessive.,D,False,0.19930872321128845,0.19930872321128845,0.10668227076530457,0.12088685482740402
Homeobox sequences,are present in the genome of many animal species,are found in prokaryotes but not in eukaryotes,were identified as the integration sites for bacterial viruses,represent integration sites for transposable elements,A,False,0.1559809446334839,0.08349058777093887,0.09460723400115967,0.176749587059021
Which of the following karyotypes is diagnostic of Down syndrome,"46,XX,der(14;21)(q10;q10)pat+21","47,XY,+13","45,XX,rob,(14;21)(q10;q10)","46,XY,t(2;3)(q21;q12)",A,True,0.18174855411052704,0.12491384148597717,0.12491384148597717,0.18174855411052704
"Nature is more important for ______ differences, while nurture has greater influence on ______ differences.",structural and anatomical; psychological and social,psychological and social; structural and anatomical,structural and psychological; anatomical and social,social and anatomical; psychological and structural,A,True,0.19197027385234833,0.08002510666847229,0.06232362240552902,0.07062190771102905
Which of the following would result in Angelman syndrome?,Maternal UPD 15,Paternal UPD 15,Deletion in the paternally derived chromosome 15,A mutation in the SNRPN promoter,B,False,0.17679235339164734,0.10722999274730682,0.12150748074054718,0.13768602907657623
Recombinant alpha-iduronidase is used for the treatment of which disease/syndrome?,Fabry disease,Gaucher disease,Hurler syndrome,Pompe disease,C,False,0.29328975081443787,0.15698669850826263,0.08402892202138901,0.10789528489112854
Research from Moshe Szyf and colleagues has provided significant findings on the epigenetic influences of prenatal maternal stress. This work has been labelled ______.,developmental epigenetics,social epigenetics,fetal epigenetics,maternal epigenetics,B,False,0.18427307903766632,0.0986342653632164,0.05982470512390137,0.14351202547550201
If both parents are affected with the same autosomal recessive disorder then the probability that each of their children will be affected equals ___.,1 in 4,1 in 2,2 in 3,1,D,False,0.18581032752990723,0.11269965767860413,0.09945710748434067,0.14470922946929932
The mutational mechanism in δβ-thalassaemia consists of:,a deletion.,a duplication.,an insertion.,a point mutation.,A,True,0.19636189937591553,0.11909951269626617,0.1051049456000328,0.15292680263519287
"Assuming Hardy-Weinberg equilibrium, the genoypte frequency of heterozygotes, if the frequency of the two alleles at the gene being studied are 0.6 and 0.4, will be:",0.8,0.64,0.48,0.32,C,False,0.1438521146774292,0.1438521146774292,0.1438521146774292,0.18470975756645203
Familial hypercholesterolaemia is caused by mutations in the gene which encodes what?,High density lipoprotein,HMG-CoA reductase,Low density lipoprotein,Low density lipoprotein receptor,D,False,0.24908576905727386,0.15107816457748413,0.10383439809083939,0.15107816457748413
A cross between two true breeding lines one with dark blue flowers and one with bright white flowers produces F1 offspring that are light blue. When the F1 progeny are selfed a 1:2:1 ratio of dark blue to light blue to white flowers is observed. What genetic phenomenon is consistent with these results?,epistasis,incomplete dominance,codominance,inbreeding depression,B,False,0.26827335357666016,0.11183296144008636,0.14359638094902039,0.05282615125179291
The proportion of babies that have an abnormality identifiable at birth is _____.,1 in 10,1 in 40,1 in 100,1 in 500,B,False,0.12209413945674896,0.09508702158927917,0.12209413945674896,0.17764592170715332
______ explained genetic disorders such as alkaptonuria and albinism.,Recessive inheritance has,Dominant genes have,X chromosomes,Y chromosomes,A,True,0.18230313062667847,0.07599525153636932,0.1252949982881546,0.1105724349617958
Which of the following conditions shows anticipation in paternal transmission?,Huntington disease,Marfan syndrome,Cystic fibrosis,Fragile X syndrome,A,False,0.145616352558136,0.145616352558136,0.18697509169578552,0.18697509169578552
A homeotic mutation is one which,is present in only one form in an individual,substitutes one body part for another in development,results in development of a tumor,is wild type at one temperature and abnormal at another,B,False,0.19157451391220093,0.11619583517313004,0.1025424525141716,0.1316671073436737
Which of the following is not a familial cancer syndrome,Familial adenomatous polyposis,Li-Fraumeni syndrome,Von Hippel-Lindau syndrome,Waardenburg syndrome,D,True,0.10375557839870453,0.10375557839870453,0.15096347033977509,0.21965055167675018
"The epigenetic inheritance system has been described as ______ (Mayr and Provine, 1980).",genotype inheritance,soft inheritance,RNA inheritance,hard inheritance,B,False,0.11089971661567688,0.1256658285856247,0.08636878430843353,0.16135813295841217
Severe anaemia at birth is a feature of what?,Alpha-thalassaemia,Beta-thalassaemia,Hereditary persistence of fetal haemoglobin,Sickle cell disease,A,True,0.19705720245838165,0.1354353129863739,0.10547711700201035,0.1534683108329773
"If an X-linked recessive disorder is in Hardy-Weinberg equilibrium and the incidence in males equals 1 in 100, then the expected incidence of affected homozygous females would be _______.",1 in 1000,1 in 4000,1 in 10 000,1 in 40 000,C,False,0.12306087464094162,0.12306087464094162,0.10860083997249603,0.17905250191688538
Tay-Sachs disease is caused by deficiency of _________________?,Alpha-L-iduronidase,Glucose-6-phosphatase,Hexosaminidase A,Homogentisic acid oxidase,C,False,0.276768296957016,0.08985351026058197,0.14814339578151703,0.10181737691164017
A nonsense mutation involves:,a regulatory sequence.,an AG splice acceptor site.,the creation of a different amino acid.,the creation of a stop codon.,D,False,0.09364303946495056,0.082639679312706,0.2246379405260086,0.19824229180812836
The polymerase chain reaction or PCR is a technique that,was used to demonstrate DNA as the genetic material,is used to determine the content of minerals in a soil sample,uses short DNA primers and a thermostable DNA polymerase to replicate specific DNA sequences in vitro.,measures the ribosome transfer rate during translation,C,True,0.08492612838745117,0.08492612838745117,0.38061249256134033,0.09623391181230545
The maternal serum level of alpha-fetoprotein (AFP) is lower than average in which situation?,Down syndrome,Exomphalos,Neural tube defects,Twin pregnancies,A,True,0.16583757102489471,0.11397837847471237,0.12915442883968353,0.16583757102489471
"______ has been described as the phenomenon by which one genotype can give rise to a range of different physiological or morphological states in response to different environmental conditions during development (West-Eberhard, 1989).",Fetal plasticity,The fetal origins hypothesis,Developmental plasticity,Environmental plasticity,C,False,0.12826690077781677,0.14534543454647064,0.11319514364004135,0.18662723898887634
Arabidopsis is advantageous for plant genetic research because:,it is commercially important as a food crop,it is an endangered species,it is the closest to humans of any existing plant,it is a small plant with a small genome size which can be raised inexpensively,D,True,0.06898345798254013,0.06898345798254013,0.11373450607061386,0.3091624081134796
The proportion of genes shared by first cousins is on average ___.,1.0/2,1.0/4,1.0/8,1.0/16,C,False,0.13350142538547516,0.13350142538547516,0.13350142538547516,0.1942434310913086
Which of the following is not a tumour suppressor gene?,APC,NF1,RB1,RET,D,True,0.13316373527050018,0.07127740979194641,0.13316373527050018,0.24878260493278503
Which of the following is a feature of X-linked dominant inheritance?,Parental consanguinity,Male to male transmission,Transmission only by females,Transmitted by males only to females,D,False,0.19943636655807495,0.12096427381038666,0.10675060003995895,0.19943636655807495
"On average, how many fragments would a restriction enzyme which recognizes a specific 4 base sequence in DNA be expected to cleave a double-stranded bacteriophage with a genome size of 5,000 bp into?",about 2,about 4,about 20,about 50,C,False,0.1738995760679245,0.11951932311058044,0.10547543317079544,0.11951932311058044
Positional cloning refers to,using a selection procedure to clone a cDNA,cloning a portion of a gene using PCR,isolating a gene by PCR using primers from another species,mapping a gene to a chromosomal region and then identifying and cloning a genomic copy of the gene from the region,D,True,0.04360004886984825,0.08145561069250107,0.07188432663679123,0.413665771484375
Plasmid vectors for cloning,can generally accommodate larger inserts than phage vectors can,"grow within bacteria, and are present in bacterial colonies on an agar plate",can accommodate inserts of over 100 kilobases,include centromeres to allow propagation in yeast,B,False,0.1592768281698227,0.09660626947879791,0.07523702830076218,0.12404490262269974
Transcriptional activator proteins,bind regions near a eukaryotic gene and allow an RNA polymerase to transcribe a gene,bind to ribosomes to activate the production of specific proteins,are produced during an infection of bacteria by a phage,are essential to function of transfer RNAs during translation,A,True,0.20911617577075958,0.09877947717905045,0.07692953199148178,0.11193181574344635
"Assuming that the level of glucose is low, a mutation in the repressor associated with the lac operon of E. coli which prevents binding of the repressor to lactose should result in: ",constitutive expression of the lac operon genes,lack of expression or reduced expression of the lac operon genes under all circumstances,expression of the genes only when lactose is present,expression of the genes only when lactose is absent,B,False,0.17269687354564667,0.15240445733070374,0.11869271844625473,0.17269687354564667
"In meiosis, recombination occurs in:",Metaphase I.,Prophase I.,Metaphase II.,Prophase II.,B,False,0.22431571781635284,0.1360543668270111,0.1200675517320633,0.09350871294736862
Leber's hereditary optic atrophy is caused by a mutation in:,chromosome 12.,chromosome 18.,chromosome 21.,mitochondrial DNA.,D,False,0.11740705370903015,0.10361137241125107,0.170826256275177,0.170826256275177
"Regarding exons, which, if any, of the following statements is correct?",Some exons in protein-coding genes consist of noncoding DNA.,The first exon of a protein-coding gene always contains the translational start site.,The last exon of a protein-coding gene always contains the normal termination codon.,A coding exon is always translated in just one of the three possible forward reading frames.,A,True,0.14088033139705658,0.09682553261518478,0.07540779560804367,0.14088033139705658
"In humans, each cell normally contains ______ of chromosomes.",11 pairs,23 pairs,32 pairs,46 pairs,B,True,0.0835837796330452,0.3305802643299103,0.04473917558789253,0.05744623392820358
"An increase in the inbreeding coefficient, F, is likely to result in:",reduced likelihood of heterozygotes being present in a population,higher proportion of genes that show linkage,higher proportion of genes with introns,higher level of difference between RNA molecules in two daughter cells,A,True,0.16918842494487762,0.10261796414852142,0.11628138273954391,0.13176408410072327
Which of the following findings on prenatal ultrasound examination would not raise suspicion of a chromosome abnormality?,Duodenal atresia,Holoprosencephaly,Hydrops fetalis,Monozygotic twins,D,True,0.1375950127840042,0.09456756711006165,0.15591557323932648,0.20019954442977905
"The likelihood of an individual in a population carrying two specific alleles of a human DNA marker, each of which has a frequency of 0.2, will be:",0.4,0.32,0.08,0.02,C,False,0.1427808552980423,0.1427808552980423,0.11119783669710159,0.20774491131305695
An Hfr strain of E. coli contains:,a vector of yeast or bacterial origin which is used to make many copies of a particular DNA sequence,a bacterial chromosome with a human gene inserted,a bacterial chromosome with the F factor inserted,a human chromosome with a transposable element inserted,C,False,0.21874651312828064,0.09118711948394775,0.08047234266996384,0.15034213662147522
Male to male transmission is a key feature of which pattern of inheritance?,Autosomal dominant,Autosomal recessive,X-linked dominant,X-linked recessive,A,True,0.18947307765483856,0.16720940172672272,0.13022281229496002,0.14756177365779877
Simple tandem repeat polymorphisms in humans are most useful for,solving criminal and paternity cases,reconstructing the relationships of humans and chimps.,estimating relationships of humans and Neanderthals,transferring disease resistance factors into bone marrow cells,A,True,0.15476736426353455,0.13658171892166138,0.12053295224905014,0.12053295224905014
Which of the following disorders is not suitable for population carrier screening?,Cystic fibrosis,Oculocutaneous albinism,Sickle cell disease,Tay-Sachs disease,B,False,0.09519635885953903,0.09519635885953903,0.15695224702358246,0.25877049565315247
Which of the following disorders does not show X-linked inheritance?,Duchenne muscular dystrophy,Tay-Sachs disease,Haemophilia A,Haemophilia B,B,False,0.13279017806053162,0.13279017806053162,0.13279017806053162,0.17050595581531525
The most common chromosome abnormality in first trimester spontaneous miscarriages is:,trisomy.,monosomy.,triploidy.,tetrasomy.,A,True,0.32889243960380554,0.12099277973175049,0.09422925859689713,0.09422925859689713
Which of the following karyotypes is not compatible with survival to birth?,"47,XY,+13","47,XX,+18","47,XY,+21","45,Y",D,True,0.13663041591644287,0.09390462934970856,0.1205759197473526,0.2552592158317566
Male breast cancer is associated with mutations in ___.,BRCA1,BRCA2,NF1,RET,B,False,0.22326995432376862,0.17388282716274261,0.10546527057886124,0.09307276457548141
Pseudocholinesterase deficiency is associated with increased sensitivity to what?,Fava beans,Halothane,Primaquine,Succinylcholine,D,True,0.16138960421085358,0.14242583513259888,0.11092135310173035,0.23482050001621246
The most common cystic fibrosis mutation consists of:,a deletion.,a duplication.,a substitution.,an insertion.,A,True,0.24270634353160858,0.10117505490779877,0.11464636772871017,0.16680946946144104
The normal human chromosome diploid number is:,23,24,46,48,C,True,0.16678208112716675,0.10115845501422882,0.21415244042873383,0.11462754756212234
Advantages of using adenoviruses for gene therapy include:,long term expression.,low risk of insertional mutagenesis.,low immunogenecity.,easy assembly.,B,False,0.16273394227027893,0.1267373263835907,0.07687006890773773,0.14361219108104706
Which of the following statements about Hirschsprung disease is incorrect?,It shows an association with Down syndrome.,It is more common in girls than in boys.,RET is a major susceptibility gene.,Recurrence risks are greater for long segment disease than for short segment disease.,B,False,0.12680813670158386,0.08715387433767319,0.11190778762102127,0.23690877854824066
Which of the following conditions is caused by a trinucleotide (triplet) repeat expansion?,Cystic fibrosis,Duchenne muscular dystrophy,Huntington disease,Osteogenesis imperfecta,C,True,0.18053081631660461,0.14059755206108093,0.20456822216510773,0.10949748009443283
Which of the following causes female pseudohermaphroditism?,Androgen insensitivity,Campomelic dysplasia,Congenital adrenal hyperplasia,Klinefelter syndrome,C,False,0.18360278010368347,0.11136071383953094,0.14298997819423676,0.18360278010368347
Which component of transcribed RNA in eukaryotes is present in the initial transcript but is removed before translation occurs?,Intron,3’ Poly A tail,Ribosome binding site,5’ cap,A,True,0.21649105846881866,0.09024690836668015,0.10226313769817352,0.14879198372364044
Which of the following is not a recognized complication of cystic fibrosis?,Cancer of the oesophagus,Congenital absence of the vas deferens,Diabetes mellitus,Liver cirrhosis,A,False,0.11483240127563477,0.10133925080299377,0.11483240127563477,0.2145351767539978
Which of the following diagnostic techniques is of no value for the diagnosis of neural tube defects?,Amniocentesis,Chorion villus sampling (CVS),Maternal serum screening,Ultrasonography,B,False,0.17016476392745972,0.13252444565296173,0.13252444565296173,0.15016986429691315
Which of the following conditions is a peroxisomal disorder?,Acute intermittent porphyria,Maple syrup urine disease,Medium chain acyl-CoA dehydrogenase deficiency,Zellweger syndrome,D,True,0.11647675931453705,0.11647675931453705,0.11647675931453705,0.2465813010931015
Marked microsatellite instability is a feature of:,familial adenomatous polyposis.,hereditary non-polyposis colon cancer (HNPCC).,multiple endocrine adenomatosis type 2.,neurofibromatosis 1.,B,True,0.17743843793869019,0.2010640799999237,0.09497594833374023,0.1565888673067093
The common mutation in α-thalassaemia consists of:,a deletion.,a duplication.,an insertion.,a point mutation.,A,True,0.23369020223617554,0.11038743704557419,0.07586810737848282,0.14174027740955353
A baby born with pulmonary hypoplasia secondary to oligohydramnios caused by renal agenesis would be classified as having:,an association.,a dysplasia.,a sequence.,a syndrome.,C,False,0.14921508729457855,0.10255392640829086,0.14921508729457855,0.19159595668315887
The ______ is the set of observable characteristics and is the sum of genetic and environmental effects.,genotype,phenotype,both genotype and phenotype,neither genotype or phenotype,B,True,0.18860465288162231,0.2744181454181671,0.054036132991313934,0.028923457488417625
Which of the following trisomy karyotypes has the mildest effect on human development?,"47,XXX","47,XXY","47,XX,+13","47,XY,+21",A,True,0.17107608914375305,0.0915704295039177,0.11757876724004745,0.17107608914375305
Mutations that cause achondroplasia exert an effect which can be classified as:,dominant negative.,gain-of-function.,haploinsufficiency.,loss-of-function.,B,False,0.07103326171636581,0.1327075958251953,0.1327075958251953,0.19308841228485107
The presence of two or more cell lines from different zygotes in a single individual is known as:,mosaicism.,diploidy.,aneuploidy.,chimaerism.,D,False,0.35237038135528564,0.0890931785106659,0.1468898206949234,0.10095580667257309
The risk for miscarriage associated with amniocentesis is approximately ____.,1 in 10,1 in 50,1 in 100 to 1 in 200,1 in 1000,C,False,0.12417563050985336,0.12417563050985336,0.14070941507816315,0.20473100244998932
Autozygosity mapping is used to map disorders that show which pattern of inheritance?,Autosomal dominant,Autosomal recessive,X-linked dominant,X-linked recessive,B,False,0.18623334169387817,0.1450386792421341,0.11295623332262039,0.1450386792421341
Consanguinity shows a strong association with which pattern of inheritance?,Autosomal dominant,Autosomal recessive,X-linked dominant,X-linked recessive,B,False,0.1950296312570572,0.15188923478126526,0.10439184308052063,0.1182914525270462
Most new mutations appear to be,beneficial,neutral or deleterious,present in homozygotes rather than heterozygotes,detectable using allozyme studies (protein electrophoresis),B,True,0.12096773087978363,0.15532565116882324,0.12096773087978363,0.15532565116882324
Twin studies in humans are useful because,they allow genetic as opposed to environmental influences on variation in a trait to be estimated,cloning of genes is facilitated by the presence of extra copies,they allow improved expression of genes,twins have a greater likelihood of being heterozygous,A,True,0.4029814898967743,0.05453761667013168,0.03748311847448349,0.0793517604470253
Complete the following sentence. The Philadelphia chromosome:,is an example of gene amplification.,is a product of a reciprocal translocation.,causes Burkitt's lymphoma.,causes retinoblastoma.,B,False,0.18369992077350616,0.1430656462907791,0.09832748025655746,0.12625497579574585
Enzyme assay can be used to identify carriers of:,Cystic fibrosis.,Fragile X syndrome.,Oculocutaneous albinism.,Tay-Sachs disease.,D,False,0.1739918738603592,0.11958274990320206,0.13550500571727753,0.15354730188846588
A high blood ammonia level occurs in:,galactosaemia.,Hurler's syndrome.,ornithine transcarbamylase (OTC) deficiency.,phenylketonuria.,C,False,0.14190377295017242,0.11051477491855621,0.14190377295017242,0.20646877586841583
"In genome-wide association studies, known SNPs explain ______ of the variation in body mass index despite the evidence of greater than 50% heritability from twin and family studies.",only 5%,less than 1%,only 13%,less than 2%,D,True,0.13294386863708496,0.10353678464889526,0.11732255667448044,0.19343218207359314
Differential distribution of substances in the egg most typically results in:,differences in gene expression which may establish a pattern in the embryo as the cells divide,amplification of specific genes during development,development of polyploid tissues,loss of specific genes during development,A,True,0.256565660238266,0.1211930438876152,0.09438524395227432,0.17633484303951263
Which of the following conditions is not caused by a mutation in FGFR3?,Achondroplasia,Crouzon syndrome,Thanatophoric dysplasia,Waardenburg syndrome,D,True,0.1072373017668724,0.09463659673929214,0.13769543170928955,0.2572489082813263