These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Robinow syndrome without mesomelic 'brachymelia': a report of five cases.
    Author: Bain MD, Winter RM, Burn J.
    Journal: J Med Genet; 1986 Aug; 23(4):350-4. PubMed ID: 3746837.
    Abstract:
    A family is described in which the father and his two children had Robinow syndrome, but with no consistent brachymelia or dwarfism. Two further sporadic cases are described, one with rhizomelic brachymelia and dwarfism and the other with generalised shortening of the limbs. An attempt is also made to distinguish between the phenotype of autosomal dominant and recessive cases on the basis of the familial cases in this paper and other reported cases.
    [Abstract] [Full Text] [Related] [New Search]