Literature DB >> 13509419

[The oligodactylia syndrome in human and its parallel mutation in the house mouse; an abnormality complex with ulnar aplasia, reduction of the ulnar marginal rays and anomalies of the intermaxillary bone, sternum, kidneys and spleen].

H WEYERS.   

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Year:  1957        PMID： 13509419

Source DB:  PubMed          Journal:  Ann Paediatr        ISSN： 0365-4966


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  3 in total

1.  Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.

Authors:  P D Turnpenny; J C Dean; P Duffty; J A Reid; P Carter
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

Review 2.  Malformation syndromes: a review of mouse/human homology.

Authors:  R M Winter
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

3.  Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly.

Authors:  P Dodinval
Journal:  Hum Genet       Date:  1979-04-27       Impact factor: 4.132
  3 in total

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