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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

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Segmental uniparental isodisomy of chromosome 6 causing transient diabetes mellitus and merosin‐deficient congenital muscular dystrophy
Segmental uniparental isodisomy (iUPD) is a rare genetic event that may cause aberrant expression of imprinted genes, and… 
2009
2009
Fetal Hydrops, Hyperechogenic Arteries and Pathological Doppler Findings at 29 Weeks: Prenatal Presentation of Generalized Arterial Calcification of Infancy – A Novel Mutation in ENPP1
Prenatal diagnosis of generalized arterial calcification of infancy (GACI) (OMIM #208000) is difficult and rare. There are… 
2005
2005
Assignment of the porcine SKI and GABRD genes to chromosome 6q22-q23.
2005
2005
Oculodentodigital dysplasia. A case report.
This report describes a rare case of oculodentodigital (ODD) dysplasia, an autosomic-dominant disease with alteration on the gene… 
2003
2003
cDNA cloning, mapping and polymorphism of the porcine Rhesus (RH) gene.
The Rhesus (Rh) gene superfamily in humans and mice contains four independent genes, RH, RHAG, RHBG, and RHCG/GK. Heretofore… 
Review
2000
Review
2000
[Genetic predisposition to bilharziasis in humans: research methods and application to the study of Schistosoma mansoni infection].
The development of genetic epidemiology methods using recent human genetic mapping information together with the growing… 
1992
1992
A study of chromosome 6 allele loss in human colorectal carcinomas.
Matched normal/tumor DNA pairs from patients with sporadic and hereditary (FAP = familial adenomatous polyposis) colorectal… 
1989
1989
Molecular mapping of the oncogene MYB and rearrangements in malignant melanoma
The human cellular oncogene MYB has been mapped to 6q22–q23. Deletions and translocations involving this region of the long arm… 
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