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5q23-q33
A chromosome band present on 5q
National Institutes of Health
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3 relations
Chromosomes
NRG2 wt Allele
chromosome 5q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
H. Azzedine
,
N. Ravisé
,
+17 authors
E. Leguern
Neurology
2006
Corpus ID: 5833708
Background: Charcot-Marie-Tooth (CMT) disease is a heterogeneous group of inherited peripheral motor and sensory neuropathies…
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Highly Cited
2003
Highly Cited
2003
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.
J. Senderek
,
C. Bergmann
,
+28 authors
K. Zerres
American Journal of Human Genetics
2003
Corpus ID: 25464261
Charcot-Marie-Tooth disease type 4C (CMT4C) is a childhood-onset demyelinating form of hereditary motor and sensory neuropathy…
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2003
2003
Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients
T. Akamizu
,
H. Hiratani
,
S. Ikegami
,
S. Rich
,
D. Bowden
Journal of Human Genetics
2003
Corpus ID: 38216299
AbstractAs part of a genome scan to locate familial Graves' disease (GD) and Hashimoto's thyroiditis (HT) genes, an autoimmune…
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Highly Cited
1999
Highly Cited
1999
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33
A. Gabreëls-Festen
,
S. V. van Beersum
,
+4 authors
E. Mariman
Journal of Neurology Neurosurgery & Psychiatry
1999
Corpus ID: 35634452
OBJECTIVES To report the occurrence of the autosomal recessive form of demyelinating Charcot-Marie-Tooth disease (CMT) with a…
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1999
1999
Secondary prevention after cerebral ischaemia of presumed arterial origin: is aspirin still the touchstone?
A. Algra
,
J. van Gijn
,
P. Koudstaal
Journal of Neurology Neurosurgery & Psychiatry
1999
Corpus ID: 20527596
I agree that, for secondary prevention of ischaemic stroke, alternatives to aspirin have to be identified,1not only because the…
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Highly Cited
1998
Highly Cited
1998
Genetic regulation of Dermatophagoides pteronyssinus-specific IgE responsiveness: a genome-wide multipoint linkage analysis in families recruited through 2 asthmatic sibs. Collaborative Study on the…
Nobuyuki Hizawa
,
L. Freidhoff
,
+10 authors
T. Beaty
Journal of Allergy and Clinical Immunology
1998
Corpus ID: 44573735
Highly Cited
1997
Highly Cited
1997
Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33
E. Leguern
,
A. Guilbot
,
+5 authors
A. Brice
Neuromuscular Disorders
1997
Corpus ID: 34331553
Highly Cited
1993
Highly Cited
1993
A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization.
D. Saltman
,
G. Dolganov
,
J. Warrington
,
J. Wasmuth
,
M. Lovett
Genomics
1993
Corpus ID: 33534703
The q23-q33 region of human chromosome 5 encodes a large number of growth factors, growth factor receptors, and hormone…
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