A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome-Reference-Cited by-同舟云学术

A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome

Published:2008-11 Issue:5 Volume:59 Page:S92-S98
ISSN:0190-9622
Container-title:Journal of the American Academy of Dermatology
language:en
Short-container-title:Journal of the American Academy of Dermatology

Author:

Castori Marco,Covaciu Claudia,Rinaldi Rosanna,Grammatico Paola,Paradisi Mauro

Publisher

Elsevier BV

Subject

Dermatology

Reference13 articles.

1. An unusual syndrome with mental retardation and sparse hair;Nicolaides;Clin Dysmorphol,1993

2. Another patient with an unusual syndrome of mental retardation and sparse hair?;Krajewska-Walasek;Clin Dysmorphol,1996

3. Nicolaides-Baraitser syndrome: confirmatory report of a syndrome with sparse hair, mental retardation, and short stature and metacarpals;Morin;Clin Dysmorphol,2003

4. Mental retardation, sparse hair, facial dysmorphism with a prominent lower lip, and lipodystrophy: a variant example of Nicolaides-Baraitser syndrome?;Witters;Genet Couns,2003

5. London dysmorphology database;Winter,2005

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1. A SMARCA2 Mutation in the First Case Report of Nicolaides-Baraitser Syndrome in Latin America: Genotype-Phenotype Correlation;Case Reports in Genetics;2017

2. Phenotype and genotype in Nicolaides-Baraitser syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2014-08-28

3. Coffin-Siris syndrome is a SWI/SNF complex disorder;Clinical Genetics;2013-07-23

4. In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome;Molecular Syndromology;2012

5. Nicolaides–Baraitser syndrome;Clinical Dysmorphology;2011-01