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7q31.3
A chromosome band present on 7q
National Institutes of Health
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Related topics
Related topics
6 relations
Chromosome 7q
Chromosomes
LEP wt Allele
SND1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss
Jian-hua Zhao
,
Sarah E. Noon
,
I. Krantz
,
Yaning Wu
American Journal of Medical Genetics. Part C…
2016
Corpus ID: 4445022
We report on a 4‐year‐old female who presented with unilateral sensorineural hearing loss and a concern for developmental delay…
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Review
2005
Review
2005
Focus on leptin, a pleiotropic hormone.
P. Fietta
Minerva Medica
2005
Corpus ID: 33171026
Leptin, the product of the obese gene located on human chromosome 7 (7q31.3), is a cytokine-type hormone mainly secreted by the…
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2005
2005
Linkage exclusion analysis of two important chromosomal regions for height.
Yan-Jun Yang
,
Yao-Zhong Liu
,
+4 authors
H. Deng
Biochemical and Biophysical Research…
2005
Corpus ID: 22154402
2004
2004
Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array‐CGH
C. Tyson
,
B. Mcgillivray
,
Chieko Chijiwa
,
E. Rajcan-Separovic
American Journal of Medical Genetics. Part A
2004
Corpus ID: 46125429
We report on a 14‐year‐old boy who presented with bilateral cleft lip and palate, hearing loss, a language processing disorder…
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2004
2004
Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32
J. Fitzgibbon
,
B. Appukuttan
,
S. Gayther
,
D. Wells
,
J. Delhanty
,
D. Hunt
Human Genetics
2004
Corpus ID: 43548690
Blue cone pigment (BCP) is one of three types of cone photoreceptors responsible for normal colour vision. In this study, the BCP…
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2004
2004
Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignancies.
M. González
,
N. Gutiérrez
,
+5 authors
J. M. Hernández
Cancer Genetics and Cytogenetics
2004
Corpus ID: 43595376
Abnormalities in the long arm of chromosome 7 are a frequent chromosomal aberration in myeloid disorders. Most studies have…
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2000
2000
Distinct allelic loss patterns in papillary serous carcinoma of the peritoneum.
Lee‐Wen Huang
,
A. Garrett
,
+5 authors
S. Mok
American Journal of Clinical Pathology
2000
Corpus ID: 21945318
Tumor and normal tissues from 55 patients with papillary serous carcinoma of the peritoneum (PSCP) were analyzed. Polymerase…
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Highly Cited
1997
Highly Cited
1997
Identification of N-WASP homologs in human and rat brain.
Maiko Fukuoka
,
Hiroaki Miki
,
Tadaomi Takenawa
Gene
1997
Corpus ID: 30183682
1995
1995
Assignment of the human protein tyrosine phosphatase, receptor-type, zeta (PTPRZ) gene to chromosome band 7q31.3.
T. Ariyama
,
K. Hasegawa
,
+4 authors
H. Yakura
Cytogenetics and Cell Genetics
1995
Corpus ID: 3270949
Human protein tyrosine phosphatase, receptor-type, zeta (PTPRZ; also denoted HPTP zeta or RPTP beta) has a large extracellular…
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1993
1993
Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3.
H. Heng
,
X. Shi
,
L. Tsui
Cytogenetics and Cell Genetics
1993
Corpus ID: 46856019
We have used the fluorescence in situ hybridization (FISH) technique to refine the localization of the cystic fibrosis…
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