TLS Online TPP Program

#Question id: 31309


Which one of the following interactions pairs plays least role in stabilizing B-DNA?

#Unit 1. Molecules and their Interaction Relevant to Biology
  1. Hydrogen bond & Hydrophobic interactions
  2. Hydrophobic interactions & Van der Wall’s interactions
  3. Ionic interactions & Hydrophobic interactions
  4. Ionic interactions & Hydrogen bonds
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TLS Online TPP Program

#Question id: 11909

#Unit 8. Inheritance Biology

In the birds, butterflies and some reptiles, sex is still chromosomal, but the male that possesses two identical sex chromosome while the female has two different sex chromosome,  in this case which one is determining  sex?

TLS Online TPP Program

#Question id: 12173

#Unit 8. Inheritance Biology

Female with only one X chromosome is a characteristics of individual with

TLS Online TPP Program

#Question id: 12487

#Unit 8. Inheritance Biology

Neurofibromatosis type 1 is one of the most common autosomal dominant disorders. A woman with neurofibromatosis type 1 has an unaffected partner. Which of the following is correct regarding their children?

TLS Online TPP Program

#Question id: 12488

#Unit 8. Inheritance Biology

Retinoblastoma usually occurs as a sporadic event but in around 10% of cases there is a positive family history due to autosomal dominant inheritance. In these families the penetrance is approximately 80% (= 0.8). A woman with retinoblastoma, whose father and grandfather were also affected, has an unaffected partner with no relevant family history. Which of the following is correct regarding their children?

TLS Online TPP Program

#Question id: 12489

#Unit 8. Inheritance Biology

Achondroplasia shows autosomal dominant inheritance with complete penetrance. A man with achondroplasia has an unaffected partner of normal height. Their first two children are not affected. Which of the following is correct?

TLS Online TPP Program

#Question id: 12490

#Unit 8. Inheritance Biology

Tay-Sachs disease shows autosomal recessive inheritance. Parents of a newly diagnosed affected child are referred for genetic counselling. It would be correct to tell them that: