Zadanie 4c
The pedigree shows a rare inherited overactivity of a gland. Discuss the most likely inheritance pattern using evidence from the diagram.
- Materiał graficzny
Deduce compatible inheritance patterns and individual genotypes from family data and discuss shared ancestry risks.
Tę umiejętność sprawdza 15 zadań wzorowanych na arkuszach IB z lat 2022–2026.
The pedigree shows a rare inherited overactivity of a gland. Discuss the most likely inheritance pattern using evidence from the diagram.
M carries an X-linked recessive haemophilia allele. N has no copy of that allele. What is the probability that the male T has haemophilia, disregarding new mutations? A. 100% B. 50% C. 0% D. 12.5%
A model pedigree concerns a fully penetrant dominant allele D causing a hereditary condition; d does not cause it. Assume no new mutation and no phenocopies. (i) Calculate the probability that individuals1 and2 have an affected child. (ii) Explain why the…
Assume complete penetrance and no new mutations. Which inheritance pattern best fits this pedigree? A. Autosomal dominant B. X-linked dominant C. Autosomal recessive D. Y-linked
The pedigree concerns an X-linked recessive condition. Let XN be the unaffected allele and Xn the condition-associated allele. Which genotype or genotypes are possible for Z? A. XnXn only B. XNXn only C. XNXN or XNXn D. XNXN or…
The model pedigree shows a fully penetrant condition caused by a dominant allele. Assume no new mutations. Which observation excludes X-linked dominant inheritance? A. Both sexes occur in the family B. Unaffected V-1 has two unaffected parents C. The affected…
Assume this model condition is controlled by one gene, has complete penetrance and involves no new mutation. Where are the condition-causing alleles in affected individuals? A. Only on the Y chromosome B. Only on one X chromosome in every affected person C. On…
State every possible genotype of the female in generation I.
Draw a Punnett grid for the possible children of couple P, using R and r.
A hypothetical condition is caused by a fully penetrant autosomal dominant allele. The pedigree shows one family; assume no new mutations. What is the probability that the next child of II-2 and II-3 will be affected? A. 0% B. 25% C. 75% D. 50%
State the probability that P has haemophilia.
This pedigree shows a fully penetrant inherited condition. Assume no new mutations. Which pattern fits it? A. Autosomal dominant inheritance B. Y-linked inheritance C. X-linked dominant inheritance D. Autosomal recessive inheritance
Draw the correct symbol and shading for X.
Calculate the probability that Y carries the variant allele.
Explain how the family group in box B excludes X-linked inheritance of this variant.
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