| Autor: |
Lurie, I., Lazjuk, G., Gurevich, D., Usoev, S. |
| Zdroj: |
Human Genetics; 1976, Vol. 32 Issue 1, p23-33, 11p |
| Abstrakt: |
An analysis of data about the+p9 syndrome revealed that this clinical entity may occur in some different genetic forms. The recurrence risk in cases with familial translocations is due to the type of meiotic segregation, 2:2 or 3:1. It was shown a nonrandomness of involvement of chromosomes 15 and 22 in translocations with chromosome number 9. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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