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 partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Author: Fryns JP, Haspeslagh M, Agneessens A, van den Berghe H.
    Journal: Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588.
    Abstract:
    In the present paper a malformed male newborn is presented with de novo 2q3 trisomy/distal 7p22 monosomy and typical clinical findings of 7p deletion syndrome including trigonocephaly.
    [Abstract] [Full Text] [Related] [New Search]