TLS Online TPP Program

#Question id: 19059


Which of the following is not used for detection in GC?

#Part-A Aptitude & General Biotechnology
  1. Infrared spectroscopy
  2. NMR
  3. Flame ionization
  4. Electrical conductivity
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TLS Online TPP Program

#Question id: 12495

#Part-A Aptitude & General Biotechnology

Haemophilia A is a severe coagulation disorder that shows X-linked recessive inheritance. Red-green colour blindness also shows X-linked recessive inheritance. A man with both haemophilia A and colour blindness is referred for genetic counseling. Assume that his partner is not a carrier of either of these conditions. Which of the following is correct?

TLS Online TPP Program

#Question id: 12496

#Part-A Aptitude & General Biotechnology

A woman who has two brothers and a maternal uncle (her mother's brother) with non-specific X-linked mental retardation is referred for genetic counselling. There are no diagnostic tests available to help determine whether or not she is a carrier. Which of the following is correct?

TLS Online TPP Program

#Question id: 12497

#Part-A Aptitude & General Biotechnology

In this pedigree A and B represent alleles at a marker locus closely linked to the disease locus. Affected individuals are shown as shaded. The disease status in III 1 is unknown. Which of the following is correct?

TLS Online TPP Program

#Question id: 12498

#Part-A Aptitude & General Biotechnology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2 and II 3 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. On the basis of the linked marker genotypes II 2 can be told that: 


TLS Online TPP Program

#Question id: 12499

#Part-A Aptitude & General Biotechnology

On the basis of the linked marker genotypes II 3 can be told that:


TLS Online TPP Program

#Question id: 12500

#Part-A Aptitude & General Biotechnology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2, II 3 and II 4 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. On the basis of the linked markers II 2 can be told that: