Chromosomal abnormalities associated with congenital contractures (arthrogryposis)-Reference-Cited by-同舟云学术

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Chromosomal abnormalities associated with congenital contractures (arthrogryposis)

Published:2008-06-28 Issue:4 Volume:27 Page:353-372
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Reed S. D.,Hall J. G.,Riccardi V. M.,Aylsworth A.,Timmons C.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb02278.x/fullpdf

Reference94 articles.

1. Monosomy 21: A possible stepwise evolution of the karyotype;Abeliovich;AJMG,1979

2. Terminal deletion of (1)(q42) and its phenotypical manifestations;Andrle;Hum. Genet.,1978

3. Case Report: Trisomy 9 syndrome;Anneren;Acta Paediatr. Scand.,1981

4. An anatomical study of Edward's syndrome;Aziz;Anat. Rec.,1979

5. Muscular and other abnormalities in a case of Edward's syndrome (18 Trisomy);Aziz;Teratol,1979

Cited by 18 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. ARTHROGRYPOSIS;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

2. Survival among children with “Lethal” congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene ( GLDN );Human Mutation;2017-08-17

3. Characterization of a group unrelated patients with arthrogryposis multiplex congenita;Jornal de Pediatria;2016-01

4. Characterization of a group unrelated patients with arthrogryposis multiplex congenita;Jornal de Pediatria (Versão em Português);2016-01

5. AMC: amyoplasia and distal arthrogryposis;Journal of Children's Orthopaedics;2015-12-01

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