Literature DB >> 4789103

Hereditary myopathy, oligophrenia, cataract, skeletal abnormalities and hypergonadotropic hypogonadism; a new syndrome.

P O Lundberg.   

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Year:  1973        PMID： 4789103     DOI： 10.1159/000114282

Source DB:  PubMed          Journal:  Eur Neurol        ISSN： 0014-3022            Impact factor:   1.710


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  2 in total

1.  Martsolf syndrome in a brother and sister: clinical features and pattern of inheritance.

Authors:  R C Hennekam; A G van de Meeberg; J M van Doorne; P F Dijkstra; J B Bijlsma
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

2.  Klinefelter syndrome and neurological disease.

Authors:  E Boltshauser; M Meyer; T Deonna
Journal:  J Neurol       Date:  1978-12-22       Impact factor: 4.849
  2 in total

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