Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 32 for Partial deletion of chromosome 9
  1. ... Hale DE, Fox PT. Myelination in children with partial deletions of chromosome ... Genet A. 2006 Feb 15;140(4):331-9. doi: 10.1002/ajmg.a.31072. Citation on ...
  2. ... located. Many cases of NMIBC tumors have a chromosome 9 deletion, which typically occurs early in tumor formation. These ... building blocks (base pairs) on one copy of chromosome 9 in each cell. The deletion occurs near the end of the long (q) ...
  3. ... chromosome mosaicism. Rarely, Turner syndrome caused by a partial deletion of the X chromosome can be passed from one generation to the ...
  4. ... Genetic Testing Registry: 3p- syndrome Distal monosomy 3p Partial deletion of the short arm of chromosome 3 National Organization for Rare Disorders (NORD) CHROMOSOME ...
  5. ... to the signs and symptoms of 22q13.3 deletion syndrome. More About This Health Condition A rearrangement (translocation) of genetic material between chromosomes 9 and 22 causes a type of cancer of ...
  6. ... called germline mosaicism. 17p- syndrome 17p11.2 monosomy Chromosome 17p deletion syndrome Deletion 17p syndrome Partial monosomy 17p SMS Genetic Testing Registry: Smith-Magenis ...
  7. ... people with trisomy 13, trisomy 21, or trisomy 9. This condition can also be associated with missing (deletions) or copied (duplications) pieces of certain chromosomes. Dandy-Walker malformation can also be a feature ...
  8. ... on PubMed Oppenheimer S, Dignan P, Soukup S. Partial trisomy 20p: familial occurrence. Am J Med Genet. 2000 Dec 11;95(4):316-9. Citation on PubMed UCSC Genome Browser: Statistics
  9. ... Li S, Mulvihill JJ, Lin HJ, Falk RE. Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals. Am J Med Genet A. 2004 Nov 1;130A(4):331-9. doi: 10.1002/ajmg.a.30156. Citation on ...
  10. ... a segment of chromosome 14 in every cell (partial trisomy 14), an extra copy of the entire chromosome in only some of the body's cells (mosaic trisomy 14), and deletions or duplications of part of chromosome 14. Full ...
previous · 1 · 2 · 3 · 4 · next