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11p13
A chromosome band present on 11p
National Institutes of Health
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Related topics
Related topics
10 relations
BDNF wt Allele
CD44 wt Allele
CD59 wt Allele
Chromosome 11 Short Arm
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Papers overview
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2014
2014
11p13 Deletion Syndrome: First Case in Morocco Detected by FISH
A. Natiq
,
Saadia Amasdl
,
+5 authors
A. Sefiani
2014
Corpus ID: 196426354
p13 deletion Syndrome or WAGR is an acronym for Wilms tumor, aniridia, genitourinary anomalies and mental retardation…
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Review
2009
Review
2009
Genotype/phenotype association in Indian congenital aniridia
G. Neethirajan
,
Abraham Solomon
,
S. Krishnadas
,
P. Vijayalakshmi
,
Periasamy Sundaresan
Indian Journal of Pediatrics
2009
Corpus ID: 29062682
The developmental birth eye disorder of iris is known as aniridia. Heterozygous PAX6 gene, which causes human aniridia and small…
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2005
2005
Loss of Heterozygosity at 11 q 22 Correlates with Low Progesterone Receptor Content in Epithelial Ovarian Cancer
Ham
,
Gabra
,
+19 authors
Smyth
2005
Corpus ID: 37383435
Forty-seven epithelial ovarian cancers were analyzed for loss of heterozygosity (LOH) at D11S35 (11q22), close to the…
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2003
2003
A submicroscopic deletion of 11p13 associated with the WAGR syndrome
G. D. de Nanclares
,
F. Martínez
,
+4 authors
L. Castaño
Clinical Genetics
2003
Corpus ID: 19852075
To the Editor: WAGR syndrome (OMIM 194072), characterized by the association of Wilms’ tumor with aniridia, ambiguous genitalia…
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1997
1997
DNA replication asynchrony between the paternal and maternal alleles of imprinted genes does not straddle the R/G transition
R. Drouin
,
M. Boutouil
,
+4 authors
N. Lemieux
Chromosoma
1997
Corpus ID: 509537
Abstract. Imprinted autosomal loci apparently reside in very large chromosomal domains that exhibit asynchrony in replication of…
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1987
1987
Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization.
G. Malpuech
,
C. Sultan
,
+4 authors
Philippe Vanlieferinghen
American journal of medical genetics
1987
Corpus ID: 36291897
A partial androgen receptor defect was found in a boy with male pseudohermaphroditism and an 11p13 deletion. We hypothesize that…
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1986
1986
[A simple method for high-resolution banding of chromosomes and its application to diagnosis of birth defects].
Y. Fukushima
[Hokkaido igaku zasshi] The Hokkaido journal of…
1986
Corpus ID: 25489316
A simple method for obtaining high-resolution banding patterns on elongated chromosomes is devised as follows: Peripheral…
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1983
1983
[Chromosome 11 and cancer].
M. Grégoire
,
C. Pernot
,
F. Himont
,
M. Pierson
,
S. Gilgenkrantz
Journal de genetique humaine
1983
Corpus ID: 9418553
Two cases with chromosome 11 anomaly related to cancer are reported. The first one has a pericentric inversion (inv. p14 q12…
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1982
1982
Status of prezygotic chromosome lesions in relation to cancer.
W. W. Nichols
Cytogenetics and Cell Genetics
1982
Corpus ID: 46796646
There are currently three recognized prezygotic chromosome defects that are associated with specific cancers. These are a…
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1981
1981
Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations.
R. Ferrell
,
V. Riccardi
Cytogenetics and Cell Genetics
1981
Corpus ID: 3222301
The gene for red blood cell (RBC) catalase has recently been mapped to 11p13, and a gene dosage effect has been demonstrated for…
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