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

Search MEDLINE/PubMed


  • Title: Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.
    Author: Syed AA, Quinton R.
    Journal: Fertil Steril; 2008 Aug; 90(2):425-6. PubMed ID: 18177653.
    Abstract:
    Congenital radioulnar synostosis is a rare skeletal defect associated with certain chromosomal abnormalities. We describe the first report of its occurrence in association with a pseudodicentric Y chromosome in a 27-year-old man with azoospermia and testicular dysfunction.
    [Abstract] [Full Text] [Related] [New Search]