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8q21.13
A chromosome band present on 8q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
FABP5 wt Allele
PAG1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Genome-wide DNA copy number profiling and bioinformatics analysis of ovarian cancer reveals key genes and pathways associated with distinct invasive/migratory capabilities
Guifen Liu
,
G. Ruan
,
Meimei Huang
,
Lili Chen
,
P. Sun
Aging
2020
Corpus ID: 209677431
Ovarian cancer (OC) metastasis presents major hurdles that must be overcome to improve patient outcomes. Recent studies have…
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2012
2012
738 Molecular Characterization of DER (8) (QTERQ21.13: PTERP23.3) Dn In a Child Associating Psychomotor Retardation, Hydrocephalus and Facial Dysmorphism
H. Hannachi
,
S. Mougou-Zerelli
,
+4 authors
A. Saâd
Archives of Disease in Childhood
2012
Corpus ID: 75464192
Complex but balanced chromosomal rearrangements can give rise, through recombination during meiosis, to complex unbalanced…
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2011
2011
Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach
S. von Spiczak
,
Katrin Finsterwalder
,
+4 authors
I. Helbig
Epilepsia
2011
Corpus ID: 7528869
Photoparoxysmal response (PPR) is a highly heritable electroencephalographic trait characterized by an increased sensitivity to…
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2011
2011
Clinical assessment and genomic landscape of a consanguineous family with three Kallmann syndrome descendants.
Shilin Zhang
,
Yan Tang
,
+9 authors
Z. Ye
Asian Journal of Andrology
2011
Corpus ID: 630221
Although some genes that cause Kallmann syndrome (KS) have been identified by traditional linkage analysis and candidate gene…
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Review
2011
Review
2011
Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies.
E. Trarbach
Asian Journal of Andrology
2011
Corpus ID: 26346787
Kallmann syndrome and normosmic isolated hypogonadotropic hypogonadism (IHH) are developmental disorders characterized by…
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2010
2010
Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis
C. D. Kovel
,
D. Pinto
,
+17 authors
B. Koeleman
Epilepsy Research
2010
Corpus ID: 9078443
2003
2003
A novel cDNA encodes a putative hRALY-like protein, hRALYL
C. Ji
,
Jin-zhong Chen
,
+8 authors
Y. Mao
Molecular Biology Reports
2003
Corpus ID: 23399484
High throughput cDNA sequencing and 5′-rapid amplification of cDNA ends (5′RACE) isolated two cDNAs that shared the same open…
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Highly Cited
1989
Highly Cited
1989
Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.
E. Haan
,
Yvonne Hull
,
S. White
,
R. Cockington
,
P. Charlton
,
D. Callen
American journal of medical genetics
1989
Corpus ID: 40396224
Here we report on a family with an inherited rearrangement of chromosome 8q, dir ins(8)(q24.11q13.3q21.13). Individuals with the…
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1988
1988
Localization of the processed gene for human ceruloplasmin to chromosome region 8q21.13----q23.1 by in situ hybridization.
H. Wang
,
M. Koschinsky
,
J. Hamerton
Cytogenetics and Cell Genetics
1988
Corpus ID: 46840476
A processed gene for human ceruloplasmin has been localized to 8q21.13---q23.1 by in situ hybridization. This result confirms the…
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