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7p13

A chromosome band present on 7p
National Institutes of Health

Related topics

Related topics

4 relations
Chromosome 7 Short ArmChromosomesGLI3 wt AlleleNPC1L1 wt Allele

Papers overview

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Highly Cited
2016
Highly Cited
2016
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation
We report a genome-wide association scan for facial features in ∼6,000 Latin Americans. We evaluated 14 traits on an ordinal… Expand
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Highly Cited
2015
Highly Cited
2015
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in… Expand
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Review
2014
Review
2014
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
Objectives Osteoarthritis (OA) is the most common form of arthritis with a clear genetic component. To identify novel loci… Expand
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2007
2007
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
BACKGROUND Endometriosis is a common disease with a heritable component. The collaborative International Endogene Study consists… Expand
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2001
2001
Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia
Deletions or monosomy of chromosomes 5 and 7 are frequently observed in myelodysplastic syndromes (MDS) and acute myelogenous… Expand
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2001
2001
Phenotype of five patients with Greig syndrome and microdeletion of 7p13.
Here we describe five patients with Greig cephalopolysyndactyly syndrome (GCPS), including one pair of monozygotic twin boys with… Expand
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Highly Cited
1998
Highly Cited
1998
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
Cerebral cavernous malformation (CCM) is a Mendelian model of stroke, characterized by focal abnormalities in small intracranial… Expand
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Highly Cited
1997
Highly Cited
1997
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
Pallister-Hall syndrome (PHS, M146510) was first described in 1980 in six newborns. It is a pleiotropic disorder of human… Expand
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Highly Cited
1997
Highly Cited
1997
Point mutations in human GLI3 cause Greig syndrome.
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… Expand
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Highly Cited
1990
Highly Cited
1990
GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.
The GLI oncogene, discovered by virtue of its amplification in human tumors, encodes a sequence-specific DNA-binding protein… Expand
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