A novel TFAP2A mutation in familial Bran
A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype
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Aliferis, Konstantinos; Stoetzel, Corinne; Pelletier, Valérie; Hellé, Sophie; An
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Article
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2011
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Informa plc
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English
⚖ 763 KB