TLS Online TPP Program

#Question id: 4756


In summer squash, white colour fruit (W) is dominant over yellow colour (w) and disc-shaped phenotype (D) is dominant over sphere-shaped phenotype (d). Determine the genotype of the parents gives 3/8 white, sphere, 3/8 white, Disk, 1/8 Yellow, Disk and 1/8 Yellow, Sphere?

#Unit 8. Inheritance Biology
  1. WwDd x WwDd           

  2. Wwdd x wwDd

  3. Wwdd x WwDd     

  4. WwDd x wwDd

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TLS Online TPP Program

#Question id: 12503

#Unit 8. Inheritance Biology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. Using the linked markers, II2 can be told that:

TLS Online TPP Program

#Question id: 12504

#Unit 8. Inheritance Biology

In this pedigree II 3 and III 1 are affected with an X-linked recessive disorder which is tightly linked to a marker locus with alleles A and B, with a recombination fraction of 0 between the disease and marker loci. Analysis of the linked marker results indicates that the disease must be segregating with:



TLS Online TPP Program

#Question id: 12505

#Unit 8. Inheritance Biology

The marker genotype for I 2 must have been:

TLS Online TPP Program

#Question id: 12506

#Unit 8. Inheritance Biology

Using the linked markers III 3 can be told that:

TLS Online TPP Program

#Question id: 12507

#Unit 8. Inheritance Biology

In this pedigree I 1 and II 2 have Becker muscular dystrophy which shows X-linked recessive inheritance. III 2 has oculocutaneous albinism which shows autosomal recessive inheritance with an incidence in the general population of 1 in 10 000. The disease status for both Becker muscular dystrophy and oculocutaneous albinism is unknown for IV 1 and IV 2.
What is the probability that III 3 is a carrier of Becker muscular dystrophy?


TLS Online TPP Program

#Question id: 12508

#Unit 8. Inheritance Biology

In this pedigree I 1 and II 2 have Becker muscular dystrophy which shows X-linked recessive inheritance. III 2 has oculocutaneous albinism which shows autosomal recessive inheritance with an incidence in the general population of 1 in 10 000. The disease status for both Becker muscular dystrophy and oculocutaneous albinism is unknown for IV 1 and IV 2.
What is the probability that III 3 is a carrier of oculocutaneous albinism?