Practice Questions

  1. Home
  2. Free Resources
  3. Practice Questions
  4. 35358
TLS Online TPP Program

#Question id: 5736

Two zygote in which one A is 44+XYY and another B is 44+XXX karyotype is best described by

#Unit 8. Inheritance Biology

  1. Non disjunction in anaphase II of spermatogenesis for A zygote while non disjunction both anaphase I and II for B zygote 

  2. Non disjunction in anaphase II of spermatogenesis for A zygote while non disjunction either anaphase I or II for B zygote 

  3. Non disjunction in anaphase II of oogenesis for A zygote while non disjunction either anaphase I or II for B zygote 

  4. Non disjunction in anaphase I of spermatogenesis for A zygote while non disjunction either anaphase I or II for B zygote 

More Questions
TLS Online TPP Program

#Question id: 5344

#Unit 8. Inheritance Biology

What is the most probable mode of inheritance depicted in the following pedigree?
TLS Online TPP Program

#Question id: 5345

#Unit 8. Inheritance Biology

Which of the following above is most probable mode of inheritance?
TLS Online TPP Program

#Question id: 5346

#Unit 8. Inheritance Biology

The following typical pedigree illustrates the key point that affected children are born to unaffected parents: Which of the following is correct statement?
TLS Online TPP Program

#Question id: 5347

#Unit 8. Inheritance Biology

The inheritance of a given disorder is recorded in small families shown below: Based on the above limited information, which one of the following inheritance pattern best explains the observations?
TLS Online TPP Program

#Question id: 5363

#Unit 8. Inheritance Biology

A Southern blot using a probe that binds to the region spanning the mutation causing albinism detects one DNA fragment in homozygous normal individuals (A/A) and two fragments in albino individuals (a/a). Following banding pattern of three offspring of parents? Which of the following correct regarding parents?
TLS Online TPP Program

#Question id: 5357

#Unit 8. Inheritance Biology

This pedigree shows the inheritance of a recessive trait in humans. Individuals that have the trait are homozygous for a recessive allele a. If H and I, who happen to be first cousins, marry and have a child, what is the chance that this child will have the recessive trait?