Duplication of the Miller-Dieker Critical Region in a Patient with a Subtelomeric Unbalanced Translocation t(10;17)(p15.3;p13.3)

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Molecular Syndromology, Vol. 3, Iss. 2, 2012-07 ,pp. : 82-88

Karger

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Point Mutations and an Intragenic Deletion in LIS1 , the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome

By Lo Nigro Cristiana   Chong Samuel S.   Smith Ann C. M.   Dobyns William B.   Carrozzo Romeo   Ledbetter David H.  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 157-164

Oxford University Press

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Isolation and embryonic expression of the novel mouse gene Hic1 , the homologue of HIC1 , a candidate gene for the Miller–Dieker syndrome

By Grimm C.   Spörle R.   Schmid T.E.   Adler I-D.   Adamski J.   Graw J.   Schughart K.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 697-710

Oxford University Press

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Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller–Dieker syndrome

By Carter Mark G.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 413-419

Oxford University Press

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Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller–Dieker syndrome

By Toyo-oka Kazuhito   Hirotsune Shinji   Gambello Michael J.   Zhou Zi-Qiang   Olson Lorin   Rosenfeld Michael G.   Eisenman Robert   Hurlin Peter   Wynshaw-Boris Anthony  

Human Molecular Genetics, Vol. 13, Iss. 10, 2004-05 ,pp. : 1057-1067

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