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Chromosome 9

Chromosomal translocation of the 4th and 20th chromosome. In genetics, a chromosome with a staining dye. See also the definition of a genetic locus.

Chromosome 9 is described in multiple online sources, as addition to our editors' articles, see section below for printable documents, Chromosome 9 books and related discussion.

Suggested Pdf Resources

DNA sequence and analysis of human chromosome 9
ANNOTATION of the CELERA HUMAN GENOME ASSEMBLY
ANNOTATION of the CELERA HUMAN GENOME ASSEMBLY - CHROMOSOME 9. 0.0Mb.
CHROMOSOME 9 400¡ 550¢ 850¢
CHROMOSOME 9. 400¡. 550¢.
Goldenhar Syndrome and Pericentric Inversion of Chromosome 9
Molecular characterization of the secondary constriction region (qh
region (qh) of human chromosome 9 is a frequent occur- rence.

Suggested News Resources

ADHD, Autism May Sometimes Share Gene Mutations
Overall, in four autism patients and two ADHD patients, the researchers discovered a cluster of rare copy number variations on chromosome 9 and around several genes necessary for the nervous system and brain development in mammals.

Suggested Web Resources

Chromosome 9 - Genetics Home Reference
Genes on chromosome 9 are among the estimated 20000 to 25000 total genes in the human How are changes in chromosome 9 related to health conditions?
Chromosome 9 - Conditions related to genes on chromosome 9
Conditions related to genes on chromosome 9.
Chromosome 9 (human) - Wikipedia, the free encyclopedia
Chromosome 9.svg. Chromosome 9 is one of the 23 pairs of chromosomes in humans.
'Gene desert' on chromosome 9 is hotspot for coronary artery
Human Chromosome 9
Nov 19, 2003 Human Chromosome Launchpad. Human Chromosome 9. No endorsement is made or implied by inclusion here.

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