Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

McGrath, John A., Duijf, Pascal H. G., Doetsch, Volker, Irvine, Alan D., de Waal, Rob, Vanmolkot, Kaate R. J., Wessagowit, Vesarat, Kelly, Alexander, Atherton, David J., Griffiths, W. Andrew D., Orlow, Seth J., van Haeringen, Arle, Ausems, Margaret G.E.M., Yang, Annie, McKeon, Frank, Bamshad, Michael A., Brunner, Han G., Hamel, Ben C. J. and van Bokhoven, Hans (2001) Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63. Human Molecular Genetics, 10 3: 221-229. doi:10.1093/hmg/10.3.221


Author McGrath, John A.
Duijf, Pascal H. G.
Doetsch, Volker
Irvine, Alan D.
de Waal, Rob
Vanmolkot, Kaate R. J.
Wessagowit, Vesarat
Kelly, Alexander
Atherton, David J.
Griffiths, W. Andrew D.
Orlow, Seth J.
van Haeringen, Arle
Ausems, Margaret G.E.M.
Yang, Annie
McKeon, Frank
Bamshad, Michael A.
Brunner, Han G.
Hamel, Ben C. J.
van Bokhoven, Hans
Title Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
Journal name Human Molecular Genetics   Check publisher's open access policy
ISSN 0964-6906
1460-2083
Publication date 2001-02-01
Year available 2001
Sub-type Article (original research)
DOI 10.1093/hmg/10.3.221
Volume 10
Issue 3
Start page 221
End page 229
Total pages 9
Place of publication Oxford, United Kingdom
Publisher Oxford University Press
Collection year 2002
Language eng
Subject 1311 Genetics
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: UQ Diamantina Institute Publications
 
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Created: Thu, 05 Dec 2013, 15:28:52 EST by Pascal Duijf on behalf of UQ Diamantina Institute