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Xq13.2
A chromosome band present on Xq.
National Institutes of Health
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2 relations
Chromosomes
XIST wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)
Jess F. Peterson
,
Donald G Basel
,
+6 authors
Ulrike P. Kappes
Journal of Pediatric Genetics
2017
Corpus ID: 3365429
Abstract We report a 19-year-old female patient with a history of short stature, primary ovarian insufficiency, sensorineural…
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2017
2017
Atypical chronic myeloid leukemia with isochromosome (X)(p10): A case report.
Masahide Yamamoto
,
Sayaka Suzuki
,
+6 authors
O. Miura
Oncology Letters
2017
Corpus ID: 25408057
Atypical chronic myeloid leukemia (aCML) is a rare subtype of myelodysplastic/myeloproliferative neoplasm (MDS/MPN). Although…
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Highly Cited
2007
Highly Cited
2007
Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas
S. Lassmann
,
R. Weis
,
+4 authors
M. Werner
Journal of molecular medicine
2007
Corpus ID: 2956635
DNA copy number changes represent molecular fingerprints of solid tumors and are as such relevant for better understanding of…
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2004
2004
Inherited tandem duplication of the X chromosome: dup(X)(q13.2-q21.2) in a family.
J. Hou
Chang Gung medical journal
2004
Corpus ID: 42437267
A 2-year-old boy who was failing to thrive and who had multiple anomalies was found to have a maternally derived tandem…
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2003
2003
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family
B. Karaman
,
Bernd Wollnik
,
H. Ermiş
,
M. Yuksel-Apak
,
S. Başaran
Prenatal Diagnosis
2003
Corpus ID: 40534646
The short‐stature homeobox‐containing gene (SHOX) on chromosome Xp22.3 was recently identified as an important determinant of the…
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1999
1999
X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.
F. Abidi
,
B. Hall
,
+6 authors
C. Schwartz
American journal of medical genetics
1999
Corpus ID: 42758707
Clinical and molecular studies are reported on a family with X-linked mental retardation (XLMR) in which there are eight affected…
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1994
1994
Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.
Paula A Clark
,
Tracy Lester
,
Laurent Villard
,
Michel Fontes
,
C. Kinnon
Journal of Medical Genetics
1994
Corpus ID: 28292082
The three microsatellite repeat loci, DXS986, DXS995, and DXS1002, have been mapped to Xq13.2-21.1. We report here their relative…
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