The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1-Reference-Cited by-同舟云学术

The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

Published:2009-06 Issue:6 Volume:84 Page:801-806
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hanson Dan,Murray Philip G.,Sud Amit,Temtamy Samia A.,Aglan Mona,Superti-Furga Andrea,Holder Sue E.,Urquhart Jill,Hilton Emma,Manson Forbes D.C.,Scambler Peter,Black Graeme C.M.,Clayton Peter E.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. The 3-M syndrome: A heritable low birthweight dwarfism;Miller;Birth Defects Orig. Artic. Ser.,1975

2. 3-M syndrome: Description of six new patients with review of the literature;Van der Wal;Clin. Dysmorphol.,2001

3. 3-M syndrome: A report of three Egyptian cases with review of the literature;Temtamy;Clin. Dysmorphol.,2006

4. Identification of mutations in CUL7 in 3-M syndrome;Huber;Nat. Genet.,2005

5. Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: New population isolate in Asia;Maksimova;J. Med. Genet.,2007

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