A pedigree of an inheritable disease is shown below.
This inheritable disease is
To determine the pattern of inheritance shown in the pedigree, let's analyze the given chart step-by-step.
In this pedigree:
Let's assess the possible inheritance patterns:
Conclusion: The pedigree shows that the disease is passed from father to son and affects males only, matching only the Y-linked pattern. Thus, the disease is only Y-linked.
Match the genetic disorder (Column I) with its molecular basis (Column II)
| Column I | Column II |
| P. Sickle-cell anemia | 1. Mutation in nucleotide excision repair |
| Q. Xeroderma pigmentosum | 2. Trisomy of chromosome 21 |
| R. Tay-Sachs disease | 3. Mutation in $ \beta$-globin gene |
| S. Down Syndrome | 4. Mutation in hexosaminidase A gene |
| Column I | Column II |
|---|---|
| P. Klinefelter Syndrome | 1. X-chromosome insufficiency |
| Q. Turner syndrome | 2. DNA helicase mutations |
| R. Bloom syndrome | 3. Nucleotide excision repair defects |
| S. Xeroderma pigmentosum | 4. Extra X chromosome(s) in a male |