Literature DB >> 9429154

Grebe syndrome: a second case with extremely severe manifestations.

M Rittler, S Higa.   

Abstract

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Year:  1997        PMID： 9429154      PMCID： PMC1051166          DOI： 10.1136/jmg.34.12.1038

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  Grebe syndrome: a very severely affected case.

Authors:  M L Kulkarni; B Kumar; A Nasser; B M Kulkarni
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

2.  Heterozygote expression in Grebe chondrodysplasia.

Authors:  D Curtis
Journal:  Clin Genet       Date:  1986-05       Impact factor: 4.438

3.  A rare genetic syndrome.

Authors:  A Quelce-Salgado
Journal:  Lancet       Date:  1968-06-29       Impact factor: 79.321

4.  Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1.

Authors:  J T Thomas; M W Kilpatrick; K Lin; L Erlacher; P Lembessis; T Costa; P Tsipouras; F P Luyten
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

5.  The femoral hypoplasia-unusual facies syndrome.

Authors:  J Burn; R M Winter; M Baraitser; C M Hall; J Fixsen
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318
  5 in total

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