Literature DB >> 5824738

Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities.

R L Weinstein, B Kliman, R E Scully.   

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Year:  1969        PMID： 5824738     DOI： 10.1056/NEJM196910302811801

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  4 in total

1.  A patient with features of both Bardet-Biedl and Alström syndromes.

Authors:  C Hauser; C Rojas; A Roth; E Schmied; J H Saurat
Journal:  Eur J Pediatr       Date:  1990-08       Impact factor: 3.183

2.  [Alström syndrome--a rare disease of diabetic association].

Authors:  B Weichenhain; J Stemplinger; A G Ziegler; W Rabl; E Standl; H Stiegler
Journal:  Med Klin (Munich)       Date:  1997-03-15

3.  Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation.

Authors:  S A Mirhosseini; L B Holmes; D S Walton
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

4.  Alström syndrome: genetics and clinical overview.

Authors:  Jan D Marshall; Pietro Maffei; Gayle B Collin; Jürgen K Naggert
Journal:  Curr Genomics       Date:  2011-05       Impact factor: 2.236
  4 in total

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