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: De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Author: Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG.
    Journal: Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721.
    Abstract:
    A newborn male infant was found to have an unusual pattern of congenital anomalies associated with an apparently balanced de novo reciprocal translocation: 46,XY,t(1;2)(p22;q22). The infant had a previously apparently undescribed multiple congenital anomalies and mental retardation syndrome.
    [Abstract] [Full Text] [Related] [New Search]