Literature DB >> 4787843

The schwartz syndrome in southern africa.

P Beighton.   

Abstract

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Mesh：

Year:  1973        PMID： 4787843     DOI： 10.1111/j.1399-0004.1973.tb01944.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  Schwartz-Jampel syndrome in two daughters of first cousins.

Authors:  L Pavone; F Mollica; A Grasso; A Cao; F Gullotta
Journal:  J Neurol Neurosurg Psychiatry       Date:  1978-02       Impact factor: 10.154

2.  Schwartz-Jampel syndrome (chondrodystrophic myotonia).

Authors:  D Viljoen; P Beighton
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

3.  Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome.

Authors:  A Richieri-Costa; S M Garcia da Silva; O Frota-Pessoa
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318
  3 in total

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