Cornelia de Lange Syndrome-Reference-Cited by-同舟云学术

Cornelia de Lange Syndrome

Published:2010 Issue: Volume: Page:113-123
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
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Author:

Liu Jinglan,Baynam Gareth

Publisher

Springer New York

Link

http://link.springer.com/content/pdf/10.1007/978-1-4419-6448-9_11.pdf

Reference124 articles.

1. Oostra RJ, Baljet B, Hennekam RC. Brachmann-de Lange syndrome “avant la lettre”. Am J Med Genet 1994; 52:267–268.

2. Brachmann W. Ein fall von symmetrischer monodactylie durch ulnadefekt, mit symmetrischer flughautbildung in den ellenbeugen, sowie anderen abnormalitaten (zwerghaftigkeit, halsrippen, behaarung). Jahrbuch Kinderheilkd 1916; 84.

3. de Lange C. Sur un type nouveau de dégénération (typus Amstelodamensis) [On a new type of degeneration (type Amsterdam)]. Arch Méd Enfants 1933; 36.

4. de Knecht-van Eekelen A, Hennekam RC. Historical study: Cornelia C. de Lange (1871–1950)—a pioneer in clinical genetics. Am J Med Genet 1994; 52:257–266.

5. Jackson L, Kline AD, Barr MA et al. de Lange syndrome: a clinical review of 310 individuals. Am J Med Genet 1993; 47:940–946.

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5. Cornelia de Lange syndrome;Radiopaedia.org;2009-11-10