.In Drosophila, the XXY condition leads to femaleness
whereas in human beings the same condition leads
to Klinefelter’s syndrome in male. It proves
(a) in human beings Y chromosome is active in sex
determination
(b) Y chromosome is active in sex determination in
both human beings and Drosophila
(c) in Drosophila Y chromosome decides femaleness
(d) Y chromosome of man have genes for syndrome.

1 Answer

Answer :

(a) in human beings Y chromosome is active in sex
determination

Related questions

Description : An abnormal human male phenotype involving an extra X-chromosome (XXY) is a case of (a) Edward’s syndrome (b) Klinefelter’s syndrome (c) intersex (d) Down’s syndrome.

Last Answer : (b) Klinefelter’s syndrome

Description : .A person with the sex chromosomes XXY suffers from (a) gynandromorphism (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Turner’s syndrome.

Last Answer : (b) Klinefelter’s syndrome

Description : Which one of the following conditions correctly describes the manner of determining the sex? (a) Homozygous sex chromosomes (ZZ) determine female sex in birds. (b) XO type of sex chromosomes ... s syndrome, determines female sex. (d) Homozygous sex chromosomes (XX) produce male in Drosophila.

Last Answer : (b) XO type of sex chromosomes determine male sex in grasshopper.

Description : .Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage? (a) Erythroblastosis fetalis - X-linked (b) Down’s syndrome - 44 autosomes + XO (c) Klinefelter’s syndrome - 44 autosomes + XXY (d) Colour blindness - Y-linked

Last Answer : (c) Klinefelter’s syndrome - 44 autosomes + XXY

Description : 5. Klinefelters syndrome has the genetic make up (a) 44 autosomes + xxy(b) 44 autosomes + xo (c) 45 autosomes + xx (d) 45 autosomes + xy

Last Answer : (a) 44 autosomes + xxy

Description : In Down’s syndrome of a male child, the sex complement is (a) XO (b) XY (c) XX (d) XXY.

Last Answer : (b) XY

Description : In Drosophila, the sex is determined by (a) the ratio of number of X-chromosome to the sets of autosomes (b) X and Y chromosomes (c) the ratio of pairs of X-chromosomes to the pairs of autosomes (d) whether the egg is fertilized or develops parthenogenetically.

Last Answer : (c) the ratio of pairs of X-chromosomes to the pairs of autosomes

Description : .In which of the following diseases, the man has an extra X-chromosome? (a) Turner’s syndrome (b) Klinefelter’s syndrome (c) Down’s syndrome (d) Haemophilia

Last Answer : (b) Klinefelter’s syndrome

Description : What is meant by ‘sex’? a. Fact of being either male or female, b. Biological and physiological characteristics that define men and women. c. Anatomical and physiological characteristics that signify the biological maleness and femaleness of an individual. d. All of the above.

Last Answer : d. All of the above.

Description : Down Syndrome, a congenital genetic disorder in human beings, is cased by : (a) a defective recessive gene in homozygous condition (b) an extra x chromosome (c) trisomy of chromosome 18 (d) trisomy of chromosome 21

Last Answer : Ans:(d)

Description : Which of the following cannot be detected in a developing fetus by amniocentesis? (a) Down’s syndrome (b) Jaundice (c) Klinefelter’s syndrome (d) Sex of the fetus

Last Answer : (b) Jaundice

Description : Explain the mechanism of sex determination in humans. Or With the help of a flow chart explain in brief how the sex of a newborn is genetically determined in human beings. Which of the two parents, the mother or the father, is responsible for determination of sex of a child? -Biology

Last Answer : Mechanism of Sex Determination in Human Beings: In human beings, the sex of the individual is genetically determined.Sex determination is the process by which sex of a new born individual can be ... happens at fertilisation. Thus, father is responsible for the determination of the sex of a child.

Description : The genes, which remain confined to differential region of ‘Y’ chromosome, are: (a) Autosomal genes (b) Holandric genes (c) Sex linked genes (d) Mutant genes

Last Answer : Ans. ((b))

Description : The colour blindness is more likely to occur in males than in females because (a) the Y-chromosome of males have the genes for distinguishing colours (b) genes for characters are located on the sex- chromosomes (c) the trait is dominant in males and recessive in females (d) none of these.

Last Answer : (b) genes for characters are located on the sex- chromosomes

Description : The genes, which remain confined to differential region of Y-chromosome, are (a) autosomal genes (b) holandric genes (c) completely sex-linked genes (d) mutant genes.

Last Answer : b) holandric genes

Description : Sex determination of child is done by whose chromosome? -General Knowledge

Last Answer : The answer is 'Father'

Description : Sex determination of child is done by whose chromosome? -General Knowledge

Last Answer : answer:

Description : Sex determination of child is done by whose chromosome? -General Knowledge

Last Answer : answer:

Description : Sex determination of child is done by whose chromosome?

Last Answer : Father

Description : 1. Sex determination of child is done by whose chromosome? 2. Who is authorised to decide over a dispute regarding disqualification of a member of Parliament? 3. Who firstly demonstrated ... of bargets, coasters and dredgers? 20. In which country was Buddhism first propogated outside India?

Last Answer : Answer : 1. Father 2. President 3. Hertz 4. Mahogany 5. Archaeological excavations 6. December 20 7. International Year of Volunteers 8. Increase growth in lenght 9. Tropical moist deciduous ... . Boxing 17. Herbert Spencer 18. During a Financial Emergency 19. Garden Reach Shipyard 20. Srilanka

Description : Assertion : Females not participate in the determination of the sex of baby . Reason : Human male is heterogametic .

Last Answer : Assertion : Females not participate in the determination of the sex of baby . Reason : Human male is ... . D. If both Assertion & Reason are False.

Description : Genetic identity of a human male is determined by (a) sex-chromosome (b) cell organelles (c) autosome (d) nucleolus.

Last Answer : a) sex-chromosome

Description : . Select the incorrect statement. (a) Human males have one of their sex-chromosome much shorter than other. (b) Male fruit fly is heterogametic. (c) In male grasshoppers, 50% of sperms have no sex-chromosome. (d) In domesticated fowls, sex of progeny depends on the type of sperm rather than egg.

Last Answer : (d) In domesticated fowls, sex of progeny depends on the type of sperm rather than egg.

Description : A fruit fly is heterozygous for sex-linked genes, when mated with normal female fruit fly, the males specific chromosome will enter egg cell in the proportion (a) 3 : 1 (b) 7 : 1 (c) 1 : 1 (d) 2 : 1.

Last Answer : (c) 1 : 1

Description : In context of amniocentesis, which of the following statements is incorrect? (a) It can be used for detection of Down’s syndrome. (b) It can be used for detection of cleft palate. (c) It is usually done when a woman is between 14-16 weeks pregnant. (d) It is used for prenatal sex determination.

Last Answer : (b) It can be used for detection of cleft palate

Description : .A human female with Turner’s syndrome (a) has 45 chromosomes with XO (b) has one additional X chromosome (c) exhibits male characters (d) is able to produce children with normal husband.

Last Answer : (a) has 45 chromosomes with XO

Description : Chromosome designation of Turner sydrome is : (1) 44A+XO (2) 44A+XXX (3) 44A+XXY (4) 44A+XYY

Last Answer : 44A+XO

Description : Lack of independent assortment of two genes A and B in fruit fly Drosophila is due to (a) repulsion (b) recombination (c) linkage (d) crossing over.

Last Answer : (c) linkage

Description : A woman proves in court that her husband was murdered by her sister, but the judge decides that the sister cannot be punished. Why? -Riddles

Last Answer : The sisters are Siamese twins.

Description : $ Those genes which are present on "Y" chromosomes of human beings are called holandric genes. ! Holandric genes are present both in men as well as wo

Last Answer : $ Those genes which are present on "Y" chromosomes of human beings are called holandric genes. ! Holandric ... wrong D. If both As and R are wrong.

Description : Read the statements given below and identify the incorrect statement. a) The human genome contains 3164.7 million nucleotide bases. b) The average gene consists of 30,000 bp c) The total number of genes is ... . d) Chromosome Y has 231 genes e) Less than 2% of the genome codes for proteins.

Last Answer : d) Chromosome Y has 231 genes

Description : Klinefelter's syndrome phenotype. -Biology

Last Answer : answer:

Description : Webbed neck is a characteristic of – (1) Down's syndrome (2) Turner's syndrome (3) Klinefelter's syndrome (4) Cri-du-chat syndrome

Last Answer : (2) Turner's syndrome Explanation: A webbed neck, or pterygium colli deformity, is a congenital skin fold that runs along the sides of the neck down to the shouldersit is a feature of Turner ... Syndrome (TS) is a condition in which a female is partly or completely missing an X chromosome.

Description : Mongolian Idiocy due to trisomy in 21st chromsome is called (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Triple X syndrome

Last Answer : (a) Down’s syndrome

Description : .A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

Last Answer : (d) Down’s syndrome.

Description : What is the genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile? (a) Down’s syndrome (b) Turner’s syndrome (c) Klinefelter’s syndrome (d) Edward syndrome

Last Answer : Klinefelter’s syndrome

Description : A disease caused by an autosomal primary non- disjunction is : (1) Klinefelter's Syndrome(2) Turner's Syndrome (3) Sickel Cell Anemia (4) Down's Syndrome

Last Answer : (4) Down's Syndrome

Description : Webbed neck is a characteristic of (1) Down’s syndrome (2) Turner’s syndrome (3) Klinefelter’s syndrome (4) Cri–du–chat syndrome

Last Answer : Turner’s syndrome

Description : Nondisjunction of a chromosome results in which of the following diagnoses? a) Down Syndrome When a pair of chromosomes fails to separate completely and creates a sperm or oocyte that contains two ... genetic condition that may occur in a single family member as a result of spontaneous mutation.

Last Answer : a) Down Syndrome When a pair of chromosomes fails to separate completely and creates a sperm or oocyte that contains two copies of a particular chromosome (nondisjunction) Down syndrome results from three number 21 chromosomes.

Description : In our society women are blamed for producing female children. Choose the correct answer for the sex-determination in humans. (a) Due to some defect like aspermia in man. (b) Due to the genetic make up of the ... . (c) Due to the genetic make up of the egg. (d) Due to some defect in the women.

Last Answer : (b) Due to the genetic make up of the particular sperm which fertilises the egg.

Description : Major Histo Compatibility Complex (MHC) is a collection of genes arrayed on A- chromosome 21 in man, chromosome 6 in mice B- chromosome 6 in man, chromosone 21 in mice C- chromosome 17in man, chromosome 6 in mice D- chromosome 6 in man, chromosome 17 in mice

Last Answer : chromosome 6 in man, chromosome 17 in mice

Description : 2. A human cell containing 22 autosomes and a Y chromosome is probably a a) somatic cell of male b) sperm cell c) somatic cell of female d) unfertilized egg cell

Last Answer : b) sperm cell

Description : In a test cross involving F1 dihybrid flies, more parental-type offspring were produced than the recombinant-type offspring. This indicates (a) the two genes are linked and present on the ... two genes are located on two different chromosomes (d) chromosomes failed to separate during meiosis.

Last Answer : (a) the two genes are linked and present on the same chromosome

Description : Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Last Answer : a) Down’s syndrome - 21st chromosome

Description : Cri-du-chat syndrome in humans is caused by the (a) trisomy of 21st chromosome (b) fertilisation of an XX egg by a normal Y-bearing sperm (c) loss of half of the short arm of chromosome 5 (d) loss of half of the long arm of chromosome 5.

Last Answer : (c) loss of half of the short arm of chromosome 5

Description : .Down’s syndrome in humans is due to (a) three ‘X’ chromosomes (b) three copies of chromosome 21 (c) monosomy (d) two ‘Y’ chromosomes.

Last Answer : b) three copies of chromosome 21

Description : If `21168=x^(4)xxy^(3)xxz^(2)`, find `(x+y+z)^((y+z)/(x+y))`, where `x, y` and `z` are positive integers.

Last Answer : If `21168=x^(4)xxy^(3)xxz^(2)`, find `(x+y+z)^((y+z)/(x+y))`, where `x, y` and `z` are positive integers.

Description : Femaleness in cucumber is induced by : a. GA b. ABA c. IBA d. None of above

Last Answer : None of above

Description : Lac operon is a cluster of genes present in (A) Human beings (B) E. coli (C) Lambda phage (D) All of these

Last Answer : Answer : B

Description : In human beings, multiple genes are involved in the inheritance of (a) sickle-cell anaemia (b) skin colour (c) colour blindness (d) phenylketonuria.

Last Answer : ) skin colour