Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome-Reference-Cited by-同舟云学术

Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome

Published:2011-05-27 Issue:7 Volume:155 Page:1716-1720
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chacon-Camacho Oscar F.,Vázquez Johanna,Zenteno Juan C.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34030/fullpdf

Reference34 articles.

1. Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome;Abo-Dalo;Am J Med Genet Part A,2007

2. No mutations in genes of the WNT signalling pathway in patients with Zimmermann-Laband syndrome;Abo-Dalo;Clin Dysmorphol,2008

3. Elephantiasis gingivae: Report of an affected family with associated hepatomegaly, soft tissue, and skeletal abnormalities;Alavandar;J All India Dent Assoc,1965

4. Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis;Anavi;Dev Med Child Neurol,1989

5. Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome;Bakeen;J Oral Pathol Med,1991

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