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: Trisomy 20p: case report and genetic review.
    Author: Lurie IW, Rumyantseva NV, Zaletajev DV, Gurevich DB, Korotkova IA.
    Journal: J Genet Hum; 1985 Jan; 33(1):67-75. PubMed ID: 3981145.
    Abstract:
    Partial trisomy for the distal part of the short arm of chromosome 20 reported in a girl aged 11/2 years with typical craniofacial dysmorphies and psychomotor retardation. The trisomy resulted from a paternal translocation t(14;20) (q32.3;p11.1). The review of 25 cases of partial trisomy 20p showed that most cases (22 : 25) were due to parental translocations. Predominant involvement of small chromosomes in translocations with chromosome 20 was also detected.
    [Abstract] [Full Text] [Related] [New Search]