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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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Related topics

3 relations
Chromosome 7 Short ArmChromosomesGLI3 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
7p13
Chromosomes
GLI3 wt Allele
Chromosome 7 Short Arm

Papers overview

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2015
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… (More)
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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… (More)
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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… (More)
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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… (More)
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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… (More)
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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… (More)
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1997
1997
Point mutations in human GLI3 cause Greig syndrome.
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… (More)
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1992
1992
Localisation of the gene for human aromatic L-amino acid decarboxylase (DDC) to chromosome 7p13-->p11 by in situ hybridisation.
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
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
The Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant disorder affecting limb and craniofacial development in… (More)
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1988
1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.
Greig cephalopolysyndactyly syndrome (GCPS) is a rare autosomal dominant form of complex polydactyly. GCPS has been tentatively… (More)
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