DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Leitch CC, Zaghloul NA, Davis EE. et al.
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
Nat Genet 2008;
40: 443-448
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