Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi syndrome.

Autor: Hoo, Joe-Jie, Chao, Margaret C., Samuel, Iris P., Morgan, Andrew M.
Zdroj: Clinical Genetics; Mar1990, Vol. 37 Issue 3, p161-166, 6p
Databáze: Complementary Index
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