Literature DB >> 4173015

A rare genetic syndrome.

A Quelce-Salgado.   

Abstract

Entities:  

Mesh：

Year:  1968        PMID： 4173015     DOI： 10.1016/s0140-6736(68)92010-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 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.  Grebe syndrome: a second case with extremely severe manifestations.

Authors:  M Rittler; S Higa
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

3.  Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias.

Authors:  H R Wiedemann; W Remagen; H A Hienz; R J Gorlin; P Maroteaux
Journal:  Z Kinderheilkd       Date:  1974

4.  A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.

Authors:  L O Langer; J Cervenka; M Camargo
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132
  4 in total

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