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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

25 related articles for article (PubMed ID: 21614993)

  • 21. Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome.
    Chen CP; Lin SP; Tsai FJ; Chern SR; Wu PC; Lee CC; Lee MS; Chen YT; Wang W
    Genet Couns; 2011; 22(1):79-83. PubMed ID: 21614993
    [No Abstract]   [Full Text] [Related]  

  • 22. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].
    Briegel W; Cohen M
    Z Kinder Jugendpsychiatr Psychother; 2004 May; 32(2):107-15. PubMed ID: 15181786
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 1q44-qter trisomy: clinical report and review of the literature.
    Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]     [New Search]
    of 2.