De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine

Autor: O’Leary, Ryan E., Shih, Jean C., Hyland, Keith, Kramer, Nancy, Asher, Y. Jane Tavyev, Graham, John M., Jr.
Zdroj: In European Journal of Medical Genetics May 2012 55(5):349-353
Databáze: ScienceDirect
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