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: A boy with severe manifestations of type A1 brachydactyly.
    Author: Slavotinek A, Donnai D.
    Journal: Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826.
    Abstract:
    We describe a male with type A1 brachydactyly, a descendant of Drinkwaters second family. In addition to absence of the middle phalanges of his hands and feet he has generalised skeletal abnormalities, nystagmus and a squint. We suggest that his clinical findings represent the more severe manifestations of this autosomal dominant gene.
    [Abstract] [Full Text] [Related] [New Search]