Holoprosencephaly due to mutations in ZIC2 : alanine tract expansion mutations may be caused by parental somatic recombination

By Sommer A.  

Human Molecular Genetics, Vol. 10, Iss. 8, 2001-04 ,pp. : 791-796

Oxford University Press

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In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation

By Brown Lucia   Paraso Melinda   Brown Stephen  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 411-420

Oxford University Press

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Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21

By Schell Ute   Wienberg Johannes   Köhler Angelika   Bray-Ward Patricia   Ward Deeann E.   Wilson William G.   Allen William P.   Lebel Robert R.   Sawyer Jeffrey R.   Campbell Paul L.   Aughton David J.   Punnett Hope H.   Lammer Edward J.   Kao Fa-Ten   Ward David C.   Muenke Maximilian  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 223-229

Oxford University Press

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A familial GLI2 deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 5, 2015-05 ,pp. : 1121-1124

John Wiley & Sons Inc

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Collective Epithelial and Mesenchymal Cell Migration During Gastrulation

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Current Genomics, Vol. 13, Iss. 4, 2012-01 ,pp. : 267-277

Bentham Science Publishers

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