Zadanie 30
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%
- Materiał graficzny
Deduce compatible inheritance patterns and individual genotypes from family data and discuss shared ancestry risks.
Tę umiejętność sprawdza 8 zadań wzorowanych na arkuszach IB z lat 2022–2026.
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%
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…
Explain what evidence in the pedigree is consistent with sex-linked inheritance.
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…
This pedigree tracks a fully penetrant X-linked recessive condition. Assume no new mutations. Which statement about the family is supported? A. I-1 must carry the allele without expressing it B. III-1 proves that an affected male cannot reach adulthood C.…
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%
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
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