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6q22-q23

A chromosome band present on 6q
National Institutes of Health

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5 relations
BCLAF1 wt AlleleChromosomesMYB geneMYB wt Allele

Papers overview

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2007
2007
A New GJA1 (Connexin 43) Mutation Causing Oculodentodigital Dysplasia Associated to Uncommon Features
Oculodentodigital dysplasia (ODDD) is an autosomal dominant disorder that includes a clinical spectrum of craniofacial… 
2005
2005
Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
BACKGROUND AND OBJECTIVES Many clinically important oncogenes and tumor suppressor genes have been identified through analysis of… 
Highly Cited
2005
Highly Cited
2005
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactyly
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 gene… 
2004
2004
A novel type of autosomal recessive syndactyly: Clinical and molecular studies in a family of Pakistani origin
Non‐syndromic syndactylies have been classified into five major types (I–V), all showing autosomal dominant mode of inheritance… 
Highly Cited
2003
Highly Cited
2003
Novel tumor suppressor loci on 6q22-23 in primary central nervous system lymphomas.
Deletions on the long arm of chromosome 6 (6q) are one of the most common chromosomal alterations in systemic high-grade non… 
Highly Cited
2003
Highly Cited
2003
IFN-γ Polymorphisms (IFN-γ +2109 and IFN-γ +3810) Are Associated with Severe Hepatic Fibrosis in Human Hepatic Schistosomiasis (Schistosoma mansoni) 1
Schistosome infection is a major public health concern affecting millions of people living in tropical regions of Africa, Asia… 
Highly Cited
1999
Highly Cited
1999
Severe hepatic fibrosis in Schistosoma mansoni infection is controlled by a major locus that is closely linked to the interferon-gamma receptor gene.
Lethal disease due to hepatic periportal fibrosis occurs in 2%-10% of subjects infected by Schistosoma mansoni in endemic regions… 
1999
1999
Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23.
Oculodentodigital dysplasia (ODDD) is an autosomal dominant condition with high penetrance and variable expressivity. The… 
Highly Cited
1996
Highly Cited
1996
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23.
Transient neonatal diabetes mellitus (TNDM) is a rare form of childhood diabetes which usually resolves in the first 6 months of… 
Highly Cited
1990
Highly Cited
1990
Plasma cell membrane glycoprotein PC-1. cDNA cloning of the human molecule, amino acid sequence, and chromosomal location.
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