Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variability.
Delahaye, A.; Sznajer, Y.; Lyonnet, S.; Elmaleh-Bergès, M.; Delpierre, I.; Audollent, S.; Wiener-Vacher, S.; Mansbach, A.-L.; Amiel, J.; Baumann, C.; Bremond-Gignac, D.; Attié-Bitach, T.; Verloes, A.; Sanlaville, D.; Clinical Genetics, 2007, vol. 72, issue 2, p 112, ISSN 00099163. ISBN 00099163.

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