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A novel filamin A D203Y mutation in a female patient with otopalatodigital type 1 syndrome and extremely skewed X chromosome inactivation

✍ Scribed by Alberto Hidalgo-Bravo; Ericka N. Pompa-Mera; Susana Kofman-Alfaro; Cesar R. Gonzalez-Bonilla; Juan Carlos Zenteno


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
115 KB
Volume
136A
Category
Article
ISSN
1552-4825

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