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2q31-q33

A chromosome band present on 2q
National Institutes of Health

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Chromosomes

Papers overview

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2006
2006
Lack of association between autism and SLC25A12.
OBJECTIVE Autism has a strong, complex genetic component, most likely involving several genes. Multiple genomic screens have… 
Highly Cited
2005
Highly Cited
2005
Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.
Type 1 diabetes is a common, multifactorial disease with strong familial clustering (genetic risk ratio [lambda(S)] approximately… 
2004
2004
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes
Highly Cited
2002
Highly Cited
2002
ORMDL proteins are a conserved new family of endoplasmic reticulum membrane proteins
BackgroundAnnotations of completely sequenced genomes reveal that nearly half of the genes identified are of unknown function… 
Highly Cited
2000
Highly Cited
2000
Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33.
Familial primary pulmonary hypertension (PPH) is a rare autosomal dominant disease characterized by distinctive changes in… 
2000
2000
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.
Primary pulmonary hypertension (PPH), an often fatal disorder, is characterized by sustained elevation of pulmonary artery… 
Highly Cited
1999
Highly Cited
1999
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.
Graves' disease (GD) is an autoimmune thyroid disorder that is inherited as a complex trait. We have genotyped 77 affected sib… 
Review
1998
Review
1998
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.
This review summarizes reports of recurrent DNA sequence copy number amplifications in human neoplasms detected by comparative… 
1998
1998
A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disease. To date, mutations in four members of the… 
Highly Cited
1996
Highly Cited
1996
Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8.
Previous genome-wide mapping studies have provided suggestive linkage evidence for several novel susceptibility loci responsible… 
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