Literature DB >> 13739303

Arthrogryposis multiplex congenita with Pierre-Robin syndrome.

L RAMAKUMAR, S C SOOD.   

Abstract

Entities:  

Keywords:  ABNORMALITIES/case reports

Mesh:

Year:  1961        PMID: 13739303     DOI: 10.1007/bf02760002

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


× No keyword cloud information.
  1 in total

1.  Amyoplasia congenita associated with hyperostosis frontalis interna.

Authors:  R N HERSON
Journal:  Br Med J       Date:  1947-09-27
  1 in total
  4 in total

1.  ARTHROGRYPOSIS CONGENITA.

Authors:  S GUPTA
Journal:  Indian J Pediatr       Date:  1964-04       Impact factor: 1.967

2.  Arthrogryposis multiplex congenita. Report of two cases.

Authors:  S Inamdar; B N Wala; R K Mansharamani; S Husain
Journal:  Indian J Pediatr       Date:  1967-12       Impact factor: 1.967

3.  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

Review 4.  A family with severe X-linked arthrogryposis.

Authors:  R C Hennekam; P G Barth; W Van Lookeren Campagne; M De Visser; K P Dingemans
Journal:  Eur J Pediatr       Date:  1991-07       Impact factor: 3.183

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.