Campomelic dysplasia: evidence of autosomal dominant inheritance.-Reference-Cited by-同舟云学术

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Campomelic dysplasia: evidence of autosomal dominant inheritance.

Published:1993-08-01 Issue:8 Volume:30 Page:683-686
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Lynch S A,Gaunt M L,Minford A M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Campomelic dysplasia. In: Radiology of syndromes, metabolic disorders and skeletal dysplasias;Taybi, H.; Lachman, R.S.,1990

2. Campomelic dysplasia; further elucidation of a distinct entity;Hall, B.D.; Spranger, J.W.;Am 7 Dis Child,1980

3. The campomelic syndrome: review, report of 17 cases, and follow up on the currently 17-year-old boy first reported by Maroteaux et al in 1971. Am7Med Genet;Houston, C.S.; Opitz, J.M.; Spranger, J.W.,1983

4. 211970 Camptomelic dwarfism. In: Mendelian inheritance in man;McKusick, V.,1990

5. Autosomal recessive inheritance in camptomelic dwarfism;Cremin, B.J.; Orsmond, G.; Beighton, P.;Lancet,1973

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1. Campomelic Dysplasia;Atlas of Genetic Diagnosis and Counseling;2017

2. Campomelic Dysplasia;Atlas of Genetic Diagnosis and Counseling;2016

3. Campomelic dysplasia;Journal of Pediatric Orthopaedics B;2014-09

4. Chondrodysplasias;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

5. Campomelic Dysplasia;Atlas of Genetic Diagnosis and Counseling;2012

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