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Xq27
A chromosome band present on Xq
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
MCF2 gene
MCF2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Dynamic structure of the SPANX gene cluster mapped to the prostate cancer susceptibility locus HPCX at Xq27.
N. Kouprina
,
A. Pavlícek
,
+9 authors
V. Larionov
Genome Research
2005
Corpus ID: 7974650
Genetic linkage studies indicate that germline variations in a gene or genes on chromosome Xq27-28 are implicated in prostate…
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Highly Cited
2005
Highly Cited
2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.
M. Bowl
,
Andrew Nesbit
,
+11 authors
M. Whyte
Journal of Clinical Investigation
2005
Corpus ID: 15945337
X-linked recessive hypoparathyroidism, due to parathyroid agenesis, has been mapped to a 906-kb region on Xq27 that contains 3…
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Highly Cited
2004
Highly Cited
2004
A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27
Hui Shen
,
Y. Zhang
,
+14 authors
H. Deng
Journal of Medical Genetics
2004
Corpus ID: 7524053
Background: Osteoporosis is a major public health problem, mainly quantified by low bone mineral density (BMD). The majority of…
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Highly Cited
2000
Highly Cited
2000
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours
E. Rapley
,
G. Crockford
,
+25 authors
D. Bishop
Nature Genetics
2000
Corpus ID: 9095109
Testicular germ-cell tumours (TGCT) affect 1 in 500 men and are the most common cancer in males aged 15–40 in Western European…
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2000
2000
Genetic Linkage Analysis of Prostate Cancer Families to Xq27–28
M. Peters
,
G. Jarvik
,
+9 authors
J. Stanford
Human Heredity
2000
Corpus ID: 13368256
Objectives: A recent linkage analysis of 360 families at high risk for prostate cancer identified the q27–28 region on chromosome…
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1999
1999
Characterization of a brain-specific nuclear LIM domain protein (FHL1B) which is an alternatively spliced variant of FHL1.
S. M. Lee
,
H. Li
,
+8 authors
C. Lee
Gene
1999
Corpus ID: 32587502
Highly Cited
1993
Highly Cited
1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
M. Hirst
,
A. Barnicoat
,
+5 authors
Martin Bobrow
Human Molecular Genetics
1993
Corpus ID: 35099864
FRAXA is unique amongst fragile sites in that it is intimately involved with a specific clinical phenotype, the fragile X…
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Highly Cited
1987
Highly Cited
1987
Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation.
C. Laird
Genetics
1987
Corpus ID: 11093800
A mechanism is proposed for the inheritance and expression of the fragile-X-linked syndrome of mental retardation in humans. Two…
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1987
1987
Increased sister chromatid exchange frequency at Xq27 site in affected fragile X males.
S. Wenger
,
J. Hennessey
,
M. Steele
American journal of medical genetics
1987
Corpus ID: 31814372
Sister chromatid exchange (SCE) was evaluated in peripheral blood lymphocytes cultured from normal subjects, fragile X carrier…
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Highly Cited
1979
Highly Cited
1979
Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.
G. Sutherland
American Journal of Human Genetics
1979
Corpus ID: 10749104
The expression of heritable fragile sites on human chromosomes has been shown to be dependent upon composition of the tissue…
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