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4q35
A chromosome band present on 4q
National Institutes of Health
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Related topics
5 relations
Chromosomes
FAT wt Allele
KLKB1 wt Allele
SLC25A4 wt Allele
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Papers overview
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2010
2010
Distinct inter-and intramuscular features observed by MR imaging and spectroscopy in patients with FSHD uncover pathobiological processes in disease development
B. Janssen
,
R. Arts
,
N. Voet
,
C. Nabuurs
,
B. Engelen
,
A. Heerschap
2010
Corpus ID: 46938480
Introduction: Facioscapulohumaral dystrophy (FSHD) is the third most common muscular dystrophy with a prevalence of 1:20000. FSHD…
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2007
2007
Identification of Quantitative Trait Loci (QTL) for canine hip dysplasia in German shepherd dogs
Y. Marschall
2007
Corpus ID: 164307614
The aim of this work was to identify quantitative trait loci (QTL) for canine hip dysplasia (CHD) in the German shepherd dog…
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2005
2005
[First facioscapulohumeral muscular dystrophy prenatal diagnosis in a Bulgarian family].
B. T. Buzhkov
,
R. Vŭzharova
,
+5 authors
B. Bakker
Akusherstvo i ginekologiia
2005
Corpus ID: 20049747
Facioscapulohumeral muscular dystrophy (FSHD) is the third most common myopathy. It is characterized by progressive descendent…
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2005
2005
Genetic heterogeneity in South African facioscapulohumeral muscular dystrophy (FSHD) families
A. V. D. Merwe
2005
Corpus ID: 83033567
FSHD is the third most common inherited disorder of muscle after Duchenne and Myotonic dystrophy. On a clinical level FSHD is…
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2002
2002
Myology News
L. Priano
,
G. Traversa
,
+10 authors
Jakubiec-Puka
2002
Corpus ID: 48844608
In October 2001 at Camogli the First National Congress of the Italian Association of Myology (Associazione Italiana di Miologia…
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1994
1994
4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy
Muscular Dystrophy
,
MD MB Peter W. Kaplan
,
+8 authors
MD L. Felicetti
Annals of Neurology
1994
Corpus ID: 33551037
In adrenoleukodystrophy, there is a variable correlation of an abnormally raised very long-chain fatty acid (VLCFA) level to the…
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1994
1994
Gene search in the FSHD region on 4q35
J. V. Deutekom
,
S. Romberg
,
M. L. Geel
1994
Corpus ID: 81687053
In the search for the FSHD gene on 4q35, four overlapping cosmids spanning a region of 95 kb including the deletion-prone…
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1994
1994
Isolation and characterization of two overlapping cosmid clones from the 4q35 region, near the facioscapulohumeral muscular dystrophy locus
G. Deidda
,
P. Grisanti
,
E. Vigneti
1994
Corpus ID: 82447542
The gene for facioscapulohumeral muscular dystrophy (FSHD) has been localized by linkage analysis to the 4q35 region. The most…
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1981
1981
A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
O. Andersen
,
C. Lundsteen
,
E. Niebuhr
Cytogenetics and Cell Genetics
1981
Corpus ID: 46765328
A complex four-break rearrangement between chromosomes 4 and 13 was ascertained in a 10-year-old mentally retarded girl. The…
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1977
1977
[Ring of the chromosome 4. I - With 4p- phenotype].
J. Fraisse
,
B. Lauras
,
J. Couturier
,
F. Freycon
Annales de Genetique
1977
Corpus ID: 22974295
A ring chromosome derived from a No. 4 chromosome was found in the complement of an 8-year-old boy with mental retardation and…
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