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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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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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

Oxford University Press

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A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3

By Chong Samuel S.   Pack Svetlana D.   Roschke Anna V.   Tanigami Akira   Carrozzo Romeo   Smith Ann C. M.   Dobyns William B.   Ledbetter David H.  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 147-155

Oxford University Press

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The Murine Homologue of HIRA, a DiGeorge Syndrome Candidate Gene, Is Expressed in Embryonic Structures Affected in Human CATCH22 Patients

By Wilming Laurens G.   Snoeren C. A. Sylvia   van Rijswijk Angelique   Grosveld Frank   Meijers Carel  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 247-258

Oxford University Press

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