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A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter

  • Published:1997-11 Issue:5 Volume:61 Page:1139-1143
  • ISSN:0002-9297
  • Container-title:The American Journal of Human Genetics
  • language:en
  • Short-container-title:The American Journal of Human Genetics

Author:

Shohat Mordechai,Lotan Rona,Magal Nurit,Shohat Tamar,Fischel-Ghodsian Nathan,Rotter Jerome I.,Jaber Lutfi

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Étude anatomique d'un case d'arthrogrypose multiple congénitale et familiale;Bargeton;Rev Neurol,1961

2. Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association;Burglen;J Clin Invest,1996

3. A comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

4. Cerebral lesions in arthrogryposis multiplex congenita;Ek;Acta Paediatr,1958

5. Familiaere arthrogryposis multiplex congenita;Frischknecht;Helv Paediatr,1960

Cited by 21 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. Research platform for children with arthrogryposis multiplex congenita: Findings from the pilot registry;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-07-29

2. Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type;Clinical Genetics;2017-07-26

3. Arthrogryposes (Multiple Congenital Contractures);Emery and Rimoin's Principles and Practice of Medical Genetics;2013

4. The Application of Three-dimensional Ultrasonography in the Prenatal Diagnosis of Arthrogryposis;Taiwanese Journal of Obstetrics and Gynecology;2008-03

5. THE FETAL MUSCULOSKELETAL SYSTEM;Ultrasonography in Obstetrics and Gynecology;2008
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