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7p13

A chromosome band present on 7p
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
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
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
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
BACKGROUND Endometriosis is a common disease with a heritable component. The collaborative International Endogene Study consists… Expand
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2001
2001
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
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
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
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
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
The GLI oncogene, discovered by virtue of its amplification in human tumors, encodes a sequence-specific DNA-binding protein… Expand
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