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.
    Author: Singh SK, Bhadada SK, Singh R, Sinha SK, Singh SK, Agrawal JK.
    Journal: J Assoc Physicians India; 2000 Aug; 48(8):836-7. PubMed ID: 11273483.
    Abstract:
    Robinow syndrome is a rare congenital abnormality. It is characterized by mesomelic brachymelia, hemivertebrae, dysmorphic facies, genital hypoplasia, micropenis, clinodactyly, camptodactly, hypoplastic nails and moderate short stature. We are documenting the case on the account of its rarity and additional features.
    [Abstract] [Full Text] [Related] [New Search]