Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome-Reference-Cited by-同舟云学术

Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome

Published:2010-08 Issue:2 Volume:87 Page:289-296
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Tukel Turgut,Šošić Dražen,Al-Gazali Lihadh I.,Erazo Mónica,Casasnovas Jose,Franco Hector L.,Richardson James A.,Olson Eric N.,Cadilla Carmen L.,Desnick Robert J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. The focal facial dermal dysplasias: report of a kindred and a proposed new classification;Kowalski;J. Am. Acad. Dermatol.,1992

2. Hereditaerer symmetrischer systematisierter Naevus aplasticus bei 38 Personem;Brauer;Dermatol. Wochenschr.,1929

3. Congenital ectodermal dysplasia of the face;Setleis;Pediatrics,1963

4. Setleis bitemporal “forceps marks” syndrome and its pathogenesis: a case report;Matsumoto;Acta Paediatr. Jpn.,1991

5. Absent meibomian glands in Setleis syndrome;Suñer;J. Pediatr. Ophthalmol. Strabismus,1997

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