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The Opitz Syndrome Gene Product, MID1, Associates with Microtubules

Opitz syndrome (OS) is a genetically heterogeneous disorder characterized by defects of the ventral midline, including hypertelorism, cleft lip and palate, heart defects, and mental retardation. We recently identified the gene responsible for X-linked OS. The ubiquitously expressed gene product,... Full description

1st Person: Schweiger, Susann
Additional Persons: Foerster, John verfasserin; Lehmann, Tanja verfasserin; Suckow, Vanessa verfasserin; Muller, Yves A. verfasserin; Walter, Gerald verfasserin; Davies, Theresa verfasserin; Porter, Helen verfasserin; van Bokhoven, Hans verfasserin; Lunt, Peter W. verfasserin; Traub, Peter verfasserin; Ropers, Hans-Hilger verfasserin
Source: in Proceedings of the National Academy of Sciences of the United States of America Vol. 96, No. 6 (1999), p. 2794-2799
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Type of Publication: Article
Language: English
Published: 1999
Keywords: research-article
Cell Biology
Online: Volltext
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