New Syndrome? Robin sequence with facial and digital anomalies in two half-brothers by the same mother-Reference-Cited by-同舟云学术

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New Syndrome? Robin sequence with facial and digital anomalies in two half-brothers by the same mother

Published:1991-08-01 Issue:2 Volume:40 Page:167-172
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chitayat David,Meunier Catherine M.,Hodgkinson Kathy A.,Azouz Michel E.

Publisher

Wiley

Subject

Genetics (clinical)

Reference29 articles.

1. Hereditary factors in the Pierre Robin syndrome

2. Pierre Robin anomaly with an accessory metacarpal of the index fingers

3. The Stickler syndrome: Evidence for close linkage to the structural gene for type II collagen

4. Robin's Syndrome

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1. Catel–Manzke syndrome: Two new patients and a critical review of the literature;European Journal of Medical Genetics;2008-09

2. R;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

3. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

4. Stomatologische Erkrankungen und Defekte;Monogen bedingte Erbkrankheiten 2;2000

5. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3;American Journal of Medical Genetics;1999-07-30

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