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: [Heterochromatic regions of chromosomes 1, 9, 16 and Y in children with signs of embryonic development disorder].
    Author: Podugol'nikova OA, Bliumina MG.
    Journal: Genetika; 1982 Dec; 18(12):2052-4. PubMed ID: 6891360.
    Abstract:
    Some reduction of the length of C segments and their variability in chromosomes 1, 9, 16 and Y was exhibited by children having disturbances at an early stage of embryogenesis. The data obtained might suggest a certain activity of the heterochromatic regions during the embryo development. Based on these data, one may also suppose that reduction of the heterochromatin amount may affect the normal morphogenetic processes.
    [Abstract] [Full Text] [Related] [New Search]