Literature DB >> 3812598

An additional case of deletion 17p11.2.

D W Popp, C P Johnson, R F Stratton.   

Abstract

Mesh：

Year:  1987        PMID： 3812598     DOI： 10.1002/ajmg.1320260228

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  1 in total

1.  Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Authors:  F Greenberg; V Guzzetta; R Montes de Oca-Luna; R E Magenis; A C Smith; S F Richter; I Kondo; W B Dobyns; P I Patel; J R Lupski
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025
  1 in total

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