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2q31-q33

A chromosome band present on 2q
National Institutes of Health

Papers overview

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2006
2006
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 is a common, multifactorial disease with strong familial clustering (genetic risk ratio [lambda(S)] approximately… 
Highly Cited
2002
Highly Cited
2002
BackgroundAnnotations of completely sequenced genomes reveal that nearly half of the genes identified are of unknown function… 
Highly Cited
2000
Highly Cited
2000
Familial primary pulmonary hypertension (PPH) is a rare autosomal dominant disease characterized by distinctive changes in… 
2000
2000
Primary pulmonary hypertension (PPH), an often fatal disorder, is characterized by sustained elevation of pulmonary artery… 
Highly Cited
1999
Highly Cited
1999
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
This review summarizes reports of recurrent DNA sequence copy number amplifications in human neoplasms detected by comparative… 
1998
1998
Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disease. To date, mutations in four members of the… 
Highly Cited
1996
Highly Cited
1996
Previous genome-wide mapping studies have provided suggestive linkage evidence for several novel susceptibility loci responsible…