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9q22

A chromosome band present on 9q
National Institutes of Health

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6 relations
ChromosomesNFIL3 wt AlleleNR4A3 wt AlleleRNF20 wt Allele

Papers overview

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2015
2015
Clinical Presentation of a Patient with a Novel Homozygous Mutation in the TRPM6 Gene
Background Hereditary hypomagnesemia with secondary hypocalcemia (HSH) is a rare autosomal recessive disease caused by mutations… 
2014
2014
New Variant Translocation (8;9;21)(q22;p24;q22) in a Patient with Granulocytic Sarcoma Concurrent with Acute Myeloid Leukemia
Granulocytic sarcoma is a form of acute myeloid leukemia which may occur in any anatomical site. Isolated pancreatic granulocytic… 
2013
2013
- 1-Weak association between the TGFBR 1 * 6 A variant and colorectal cancer : a family-based association study on non-syndromic family members from Australia and Spain
Background Genome-wide linkage studies have identified the 9q22 chromosomal region as linked with colorectal cancer (CRC… 
2013
2013
Atención estomatológica del paciente pediátrico con síndrome de Robinow
Robinow syndrome, described in 1969 by Meinhard Robinow presents facial features similar to those seen in a fetus of about eight… 
2008
2008
7 q 31 : A Genome-Wide Analysis Common Familial Colorectal Cancer Linked to Chromosome
Present investigations suggest that f30% of colorectal cancer cases arise on the basis of inherited factors. We hypothesize that… 
2005
2005
Genetic Linkage to Human Height is Identified to 9q22 and Xq24
2003
2003
Loss of heterozygosity at 9q22-31 and examination of the PTCH tumour supressor gene in ovarian tumours.
1994
1994
Physical mapping of the Gorlin syndrome region on 9q22 by pulsed field gel electrophoresis (PFGE) and FISH
Gorlin syndrome is an autosomal dominant disorder characterized by basal cell carcinomas, medulloblastomas, and ovarian fibromas… 
1990
1990
A variant Philadelphia chromosome (Ph1) positive chronic myelocytic leukemia.
A rare case of variant Philadelphia (Ph1) chromosome positive [46, XX, t (9; 22) (q34; q11), inv (9) (9q22; 22q13)] chronic… 
1977
1977
Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
A profoundly retarded, 12-year-old female is described. Her phenotype is compatible with the clinical features of the trisomy 9p…