Katalog GES



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; Lehmann, Tanja; Suckow, Vanessa; Muller, Yves A.; Walter, Gerald; Davies, Theresa; Porter, Helen; van Bokhoven, Hans; Lunt, Peter W.; Traub, Peter; Ropers, Hans-Hilger
Source: in Proceedings of the National Academy of Sciences of the United States of America Vol. 96, No. 6 (1999), p. 2794-2799
More Articles
Type of Publication: Article
Language: English
Published: 1999
Keywords: Cell Biology
Online: Volltext
  Search for full text

Online

Volltext

Similar Items

Cannot find similar records

Library Services

Search Options

Quick links

Orientation