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A complex TFAP2A allele is associated with branchio-oculo-facial syndrome and inner ear malformation in a deaf child

✍ Scribed by Mustafa Tekin; Aslı Sırmacı; Berrin Yüksel-Konuk; Suat Fitoz; Levent Sennaroğlu

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 212 KB
Volume: 149A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32619

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