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 *

153 related articles for article (PubMed ID: 1719812)

  • 1. Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
    Surh LC; Ledbetter DH; Greenberg F
    Am J Med Genet; 1991 Oct; 41(1):15-7. PubMed ID: 1719812
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype.
    Karnitis SA; Burns K; Sudduth KW; Golden WL; Wilson WG
    Am J Med Genet; 1992 Sep; 44(2):153-7. PubMed ID: 1280909
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infant with multiple congenital anomalies and deletion (9)(q34.3).
    Schimmenti LA; Berry SA; Tuchman M; Hirsch B
    Am J Med Genet; 1994 Jun; 51(2):140-2. PubMed ID: 7522397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
    Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TB