We analyzed the possibility of inherited predisposition to nondisjunction in a family with two cases of Down syndrome using restriction fragment length polymorphisms and cytogenetic heteromorphisms. In both patients the extra chromosome 21 was the result of a nondisjunction event at first meiotic di
โฆ LIBER โฆ
Molecular analysis of the causes of down syndrome in a family
โ Scribed by Jozsef Szeberenyi
- Publisher
- The American Society for Biochemistry and Molecular Biology
- Year
- 2005
- Tongue
- English
- Weight
- 46 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1470-8175
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