Literature DB >> 13693610

Laurence-Moon-Biedl syndrome. Report of an unusual family.

E C CICCARELLI, E S VESELL.   

Abstract

Keywords:  LAURENCE-MOON-BIEDL SYNDROME/genetics

Mesh：

Year:  1961        PMID： 13693610     DOI： 10.1001/archpedi.1961.04020050109017

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  3 in total

1.  Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family.

Authors:  M Endo; Y Tasaka; N Matsuura; I Matsuda
Journal:  Eur J Pediatr       Date:  1976-11-03       Impact factor: 3.183

2.  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

3.  [Defects and excess in Laurence-Moon-Bardet-Biedl syndrome].

Authors:  G Jacobi
Journal:  Z Kinderheilkd       Date:  1965-10-11
  3 in total

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