Literature DB >> 6348506

[The Schwartz-Jampel syndrome. Description of a case with neonatal manifestations and a review of literature].

R Rosignoli, F Zanini.   

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Year:  1983        PMID： 6348506

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN： 0026-4946            Impact factor:   1.312


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  2 in total

1.  Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.

Authors:  K A Brown; L I al-Gazali; L M Moynihan; N J Lench; A F Markham; R F Mueller
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Neonatal Schwartz-Jampel syndrome: a common autosomal recessive syndrome in the United Arab Emirates.

Authors:  L I Al-Gazali; M Varghese; E Varady; J Al Talabani; J Scorer; D Bakalinova
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318
  2 in total

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