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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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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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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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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Mice defective in Trpm6 show embryonic mortality and neural tube defects

By Walder Roxanne Y.   Yang Baoli   Stokes John B.   Kirby Patricia A.   Cao Xiao   Shi Peijun   Searby Charles C.   Husted Russell F.   Sheffield Val C.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4367-4375

Oxford University Press

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