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

Cornelia de Lange syndrome

Published:2014-10-28 Issue:1 Volume:88 Page:1-12
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Boyle M.I.¹,Jespersgaard C.¹,Brøndum-Nielsen K.¹,Bisgaard A.-M.¹,Tümer Z.¹

Affiliation:

1. Applied Human Molecular Genetics, Kennedy Center, Department of Clinical Genetics, Rigshospitalet; University of Copenhagen; Glostrup Denmark

Funder

A.P. MÃ¸ller and wife Chastine Mc-Kinney MÃ¸llers Foundation (Fonden til LÃ¦gevidenskabens Fremme).

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference91 articles.

1. Sur un type nouveau de degenerescence (typus Amstelodamensis);Lange;Arch Med Enfants,1933

2. 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

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

4. Descriptive epidemiology of Cornelia de Lange syndrome in Europe;Barisic;Am J Med Genet A,2008

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