Literature DB >> 13864980

[Anatomical study of a case of congenital and familial multiple arthrogryposis].

E BARGETON, C NEZELOF, P GURAN, J C JOB.   

Abstract

Entities:  

Keywords:  JOINTS/diseases

Mesh：

Year:  1961        PMID： 13864980

Source DB:  PubMed          Journal:  Rev Obstet Ginecol Venez        ISSN： 0048-7732


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  4 in total

1.  A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Authors:  M Shohat; R Lotan; N Magal; T Shohat; N Fischel-Ghodsian; J I Rotter; L Jaber
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

2.  Arthrogryposis accompanying congenital spinal-type muscular atrophy.

Authors:  M Besser; A Behar
Journal:  Arch Dis Child       Date:  1967-12       Impact factor: 3.791

3.  A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis.

Authors:  P Fleury; G Hageman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-10       Impact factor: 10.154

4.  Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

Authors:  Z Borochowitz; B Glick; S Blazer
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318
  4 in total

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