A family with autosomal dominant distal arthrogryposis multiplex congenita and Brown syndrome-Reference-Cited by-同舟云学术

A family with autosomal dominant distal arthrogryposis multiplex congenita and Brown syndrome

Published:1999-01 Issue:4 Volume:20 Page:233-241
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Lobefalo Lucio,Mancini Adriano,Petitti Maria T.,Verrotti Alberto,Della Loggia Giuseppe,Di Muzio Antonio,Chiarelli Francesco,Gallenga Pier E.

Publisher

Swets & Zeitlinger Publishers

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1076/opge.20.4.233.2267

Reference26 articles.

1. Hall JG, Green G, Powers E. Arthrogryposis — clinical and genetic heterogeneity. Presented at the Vth Conference on Birth Defects, Montreal, August 1977.

2. An unusual distal arthrogryposis

3. Distal arthrogryposis type II: A family with varying congenital abnormalities

4. Familial distal arthrogryposis with craniofacial abnormalities: A new subtype of type II?

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