A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3

Author： Sertié A. L.   Quimby M.   Moreira E. S.   Murray J.   Zatz M.   Antonarakis S. E.   Passos-Bueno M. R.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.5, Iss.6, 1996-01, pp. : 843-847

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