Arthrogryposis Multiplex Congenita: Neurogenic Type with Autosomal Recessive Inheritance-Reference-Cited by-同舟云学术

Arthrogryposis Multiplex Congenita: Neurogenic Type with Autosomal Recessive Inheritance

Published:1974-03-01 Issue:1 Volume:11 Page:91-94
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Rosenmann A.,Arad I.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Arthrogryposis multiplex due to congenital muscular dystrophy;Banker, B.Q.; Vitcor, M.; Adams, R.D.;Brain,1957

2. etude anatomique d'un cas d'arthrogrypose multiple congenitale et familiale;Bargeton, E.; Nezelof, C.; Guran, P.; Job, J.C.;Revue Neurologique,1961

3. Arthrogryposis multiplex congenita: case due to disease of the anterior horn cells;Drachman, D.B.; Banker, B.Q.;Archives of Neurology,1961

4. Cerebral lesions in arthrogryposis multiplex congenita;Ek, J.I.;Acta Paediatrica,1958

5. Arthrogryposis multiplex congenita. A review of forty-five cases;Friedlander, H.L.; Westin, G.W.; Wood, W.L.;Journal of Bone and3Joint Surgery,1968

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