First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations.

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Published in J Med Genet on January 01, 2005

Authors

L Pasquier1, C Dubourg, M Gonzales, L Lazaro, V David, S Odent, F Encha-Razavi

Author Affiliations

1: Unité de Génétique Médicale, Hôpital SUD, Rennes, France.

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