On the Molecular Etiology of Cornelia de Lange Syndrome-Reference-Cited by-同舟云学术

On the Molecular Etiology of Cornelia de Lange Syndrome

Published:2008-12-23 Issue:1 Volume:1151 Page:22-37
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:

Author:

Dorsett Dale,Krantz Ian D.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2008.03450.x/fullpdf

Reference103 articles.

1. Ein fall von symmetrischer monodaktylie durch Ulnadefekt, mit symmetrischer flughautbildung in den ellenbeugen, sowie anderen abnormitaten (zwerghaftogkeit, halsrippen, behaarung);Brachmann;Jarb. Kinder. Phys. Erzie.,1916

2. Sur un type nouveau de dégénération (typus Amstelodamensis);De Lange;Arch. Méd. Enfants,1933

3. Brachmann-de Lange syndrome. Delineation of the clinical phenotype;Ireland;Am. J. Med. Genet.,1993

4. de Lange syndrome: a clinical review of 310 individuals;Jackson;Am. J. Med. Genet.,1993

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