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7p13
A chromosome band present on 7p
National Institutes of Health
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Related topics
Related topics
4 relations
Chromosome 7 Short Arm
Chromosomes
GLI3 wt Allele
NPC1L1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
1995
Review
1995
Genetic changes in ovarian cancer.
T. Pejovic
Annals medicus
1995
Corpus ID: 30351032
The development of cancer is a multistep process involving accumulation of genetic changes which progressively transform normal…
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1990
1990
Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.
Klaus Wagner
,
P. Kroisel
,
Walter Rosenkranz
Genomics
1990
Corpus ID: 25065783
1989
1989
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13).
H. Drabkin
,
M. Sage
,
+7 authors
F. Ruddle
Genomics
1989
Corpus ID: 22010027
Highly Cited
1989
Highly Cited
1989
Immunophenotype-karyotype associations in human acute lymphoblastic leukemia.
FM Uckun
,
K. Gajl-Peczalska
,
A. Provisor
,
NA Heerema
Blood
1989
Corpus ID: 19369050
The present study is a detailed analysis of the cytogenetic features of leukemic cells from 104 immunologically classified acute…
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1989
1989
Coincidence in fragile site expression with fluorodeoxyuridine and bromodeoxyuridine.
A. Fundia
,
I. Larripa
Cancer Genetics and Cytogenetics
1989
Corpus ID: 24976709
1989
1989
Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).
G. Krüger
,
J. Götz
,
+4 authors
L. Zech
American journal of medical genetics
1989
Corpus ID: 27074023
We report on cases of Greig syndrome segregating in a large kindred over four generations due to reciprocal translocation t(6;7…
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Highly Cited
1988
Highly Cited
1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.
L. Brueton
,
L. Brueton
,
+4 authors
J. Reynolds
American journal of medical genetics
1988
Corpus ID: 45367066
Greig cephalopolysyndactyly syndrome (GCPS) is a rare autosomal dominant form of complex polydactyly. GCPS has been tentatively…
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Review
1988
Review
1988
Microdeletion syndromes, balanced translocations, and gene mapping.
A. Schinzel
Journal of Medical Genetics
1988
Corpus ID: 2431482
High resolution prometaphase chromosome banding has allowed the detection of discrete chromosome aberrations which escaped…
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1986
1986
Possible involvement of unstable sites on chromosomes 7 and 14 in human cancer.
J. Scheres
,
T. Hustinx
,
J. Trent
Cancer Genetics and Cytogenetics
1986
Corpus ID: 22746402
Highly Cited
1984
Highly Cited
1984
The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans
N. Caccia
,
M. Kronenberg
,
+9 authors
T. Mak
Cell
1984
Corpus ID: 26615965
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