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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Abstract