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Xq27.3
A chromosome band present on Xq.
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
FMR1 wt Allele
SPANXN2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genotype-Phenotype Correlates in Fragile X Syndrome
E. Zaky
2018
Corpus ID: 55219046
Fragile X syndrome is a genetic disorder that affects both males and females but males are more severely affected than females…
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2017
2017
Síndrome del cromosoma X frágil
M. M. Castillo
,
I. E. Doménech
,
A. G. Moreno
,
L. Portilla
2017
Corpus ID: 79809044
Fragile X syndrome Fragile X syndrome (FXS) is an inherited disease linked to the X chromosome that mainly affects men and that…
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2015
2015
FRAGILE X: Mental Retardation Caused by Expanded CGC and Silenced FMR
R. Khan
2015
Corpus ID: 18921981
Clinical diagnoses of inherited mental retardation and autism encompass heterogeneous subsets of patients with differing…
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Review
2013
Review
2013
Title Deletion Xq 27 . 3 q 28 in female patient with global developmental delays and skewed X-inactivation Permalink
Lauren S. Marshall
,
J. Simon
,
+4 authors
M. Zaragoza
2013
Corpus ID: 180255508
Background: Global developmental delay and mental retardation are associated with X-linked disorders including Hunter syndrome…
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2011
2011
and Committee on Genetics Health Supervision for Children With Fragile X Syndrome
J. Hersh
,
R. Saul
2011
Corpus ID: 15903980
Fragile X syndrome (an FMR1–related disorder) is the most commonly inherited form of mental retardation. Early physical…
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2011
2011
Lectura y escritura en niños con síndrome x frágil: estrategias de intervención
María Paz Fernández Lozano
,
A. Ferreras
,
M. T. R. Lucas
2011
Corpus ID: 55151669
El sindrome X fragil (SXF) es la causa mas frecuente de discapacidad intelectual hereditaria. Se caracteriza por un fenotipo…
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2000
2000
Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers
A. Apessos
,
J. Harper
,
J. Delhanty
2000
Corpus ID: 260421675
1992
1992
Do sequences in Xq27.3 play a role in X inactivation?
M. Schmidt
American journal of medical genetics
1992
Corpus ID: 36336067
1990
1990
Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.
Tessa Webb
,
P. A. Jacobs
Journal of Medical Genetics
1990
Corpus ID: 37203935
X inactivation studies have been carried out on lymphocytes from eight unrelated females heterozygous for the Martin-Bell…
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Review
1986
Review
1986
DNA studies of X-linked mental retardation associated with a fragile site at Xq27.
Kay E. Davies
,
J. M. Opitz
,
James F. Reynolds
American journal of medical genetics
1986
Corpus ID: 12417379
X-linked mental retardation associated with expression of a fragile site at Xq27.3 has attracted much interest because…
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