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7p15.1

A chromosome band present on 7p
National Institutes of Health

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3 relations
Chromosome 7 Short ArmChromosomesNPY wt Allele

Papers overview

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2011
2011
Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.
2005
2005
Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 → pter) and partial monosomy 9p (9p22 → pter)
A 31-year-old, primigravid woman had received obstetric care in a private clinic. The pregnancy was uneventful until 34 weeks… 
Highly Cited
2003
Highly Cited
2003
Identification and characterization of the genes encoding human and mouse osteoactivin.
Osteoactivin (OA) is more highly expressed in the bones of osteopetrotic mutant rats (op/op) than in those of their normal… 
2000
2000
Comparative mapping of the human homologue of the rat diabetes susceptibility gene lyp to a 1.3-Mb segment on HSA7.
The rat diabetes susceptibility gene, Lyp or Lymphopenia, has been localized to RNO4. Proximal to Lyp are the genes caspase-2… 
1995
1995
Assignment of the human neuropeptide Y gene to chromosome 7p15.1 by nonisotopic in situ hybridization.
1990
1990
Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
Here we report on a de novo apparently balanced reciprocal 5q;7p translocation in a 15-year-old girl with apparent Cohen syndrome… 
1988
1988
Gene dosage studies regionally assign the phosphoserine phosphatase gene to 7p15.1 or 2.
Gene dosage studies in subjects with imbalances of the short arm of chromosome 7 have suggested the localization of the… 
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