A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly-Reference-Cited by-同舟云学术

A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly

Published:2008-04-23 Issue:4 Volume:26 Page:342-355
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Rozin M. M.,Hertz M.,Goodman R. M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb01070.x/fullpdf

Reference59 articles.

1. Dysmor-phogenesis of joints, brain, and palate: a new dominantly inherited syndrome;Aase;J. Pediatr.,1968

2. Kindred showing congenital absence of the dermal ridges (fingerprints) and associated anomalies;Baird;J. Pediatr.,1964

3. A new camptodactyly syndrome;Baraitser;J. Med. Genet.,1982

4. A recessively inherited windmill-vane campto-dactyly/ichthyosis syndrome;Baraitser;J. Med. Genet.,1983

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3. Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?;Clinical Genetics;2008-06-28

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5. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007