Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome-Reference-Cited by-同舟云学术

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Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome

Published:2002-10 Issue:4 Volume:11 Page:243-247
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

Figuera L.E.,Ram??rez-Due??as M.L.,D??valos I.P.,Cant?? J.M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference9 articles.

1. A familial syndrome of short stature associated with facial dysplasia and genital anomalies

2. A new camptodactyly syndrome

3. A revised and extended classification of the distal arthrogryposes

4. Guadalajara camptodactyly syndrome

5. Guadalajara camptodactyly syndrome type II

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly;PLOS ONE;2016-05-25

2. Amyoplasia involving only the upper limbs or only involving the lower limbs with review of the relevant differential diagnoses;American Journal of Medical Genetics Part A;2014-01-23

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

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