7p13

A chromosome band present on 7p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1979-2017
024619792017

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2015
2015
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in… (More)
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2007
2007
BACKGROUND Endometriosis is a common disease with a heritable component. The collaborative International Endogene Study consists… (More)
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2001
2001
Here we describe five patients with Greig cephalopolysyndactyly syndrome (GCPS), including one pair of monozygotic twin boys with… (More)
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2001
2001
Deletions or monosomy of chromosomes 5 and 7 are frequently observed in myelodysplastic syndromes (MDS) and acute myelogenous… (More)
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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… (More)
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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… (More)
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1997
1997
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… (More)
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1992
1992
The human gene for aromatic L-amino acid decarboxylase (DDC) was previously assigned to chromosome 7 by analysis of a panel of… (More)
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Highly Cited
1991
Highly Cited
1991
The Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant disorder affecting limb and craniofacial development in… (More)
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1988
1988
Greig cephalopolysyndactyly syndrome (GCPS) is a rare autosomal dominant form of complex polydactyly. GCPS has been tentatively… (More)
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