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A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype

✍ Scribed by Aliferis, Konstantinos; Stoetzel, Corinne; Pelletier, Valérie; Hellé, Sophie; Angioï-Duprez, Karine; Vigneron, Jacqueline; Leheup, Bruno; Marion, Vincent; Dollfus, Hélène

Book ID: 121877368
Publisher: Informa plc
Year: 2011
Tongue: English
Weight: 763 KB
Volume: 32
Category: Article
ISSN: 1381-6810
DOI: 10.3109/13816810.2011.592176

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