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7p13

A chromosome band present on 7p
National Institutes of Health

Papers overview

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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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2009
2009
OBJECTIVE The majority of research into functional psychosis has proceeded under the assumption that schizophrenia and bipolar… Expand
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Highly Cited
2001
Highly Cited
2001
Background Thioredoxins (Trx) are small redox proteins that function as general protein disulphide reductases and regulate… Expand
Highly Cited
2001
Highly Cited
2001
Deletions or monosomy of chromosomes 5 and 7 are frequently observed in myelodysplastic syndromes (MDS) and acute myelogenous… Expand
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Highly Cited
2000
Highly Cited
2000
Niemann-Pick type C1 (NPC1) disease is caused by defects in the NPC1 protein, which result in perturbation of subcellular… Expand
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
Highly Cited
1997
Highly Cited
1997
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… Expand
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
Highly Cited
1984
Highly Cited
1984
Homologous clones that encode the beta chain of the T cell antigen receptor have been isolated recently from both murine and… Expand