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Variability of X-linked muscular dystrophy.
1983
K H Fischbeck, and D L Schotland
Associated MeSH Terms
Cite
UI
MeSH Term
Description
Entries
D008040
Genetic Linkage
The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME.
Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D008297
Male
Males
D009136
Muscular Dystrophies
A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
Muscular Dystrophy,Myodystrophica,Myodystrophy,Dystrophies, Muscular,Dystrophy, Muscular,Myodystrophicas,Myodystrophies
D002648
Child
A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL.
Children
D002675
Child, Preschool
A child between the ages of 2 and 5.
Children, Preschool,Preschool Child,Preschool Children
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
Related Publications
K H Fischbeck, and D L Schotland
X-linked muscular dystrophy.
November 1977, Annals of neurology,
K H Fischbeck, and D L Schotland
Intrafamilial variability of X-linked progressive muscular dystrophy. Mild and acute form of X-linked muscular dystrophy in the same family.
April 1978, Journal of neurology,
K H Fischbeck, and D L Schotland
X linked muscular dystrophy with contractures.
December 1986, Journal of medical genetics,
K H Fischbeck, and D L Schotland
[X-linked Emery-Dreifuss muscular dystrophy(X-EDMD)].
January 2001, Ryoikibetsu shokogun shirizu,
K H Fischbeck, and D L Schotland
[Molecular genetics of X-linked muscular dystrophy].
July 1990, Nihon rinsho. Japanese journal of clinical medicine,
K H Fischbeck, and D L Schotland
Proteomic profiling of x-linked muscular dystrophy.
December 2009, Journal of muscle research and cell motility,
K H Fischbeck, and D L Schotland
Carrier detection in X-linked muscular dystrophy.
October 1969, Journal de genetique humaine,
K H Fischbeck, and D L Schotland
X-linked muscular dystrophy--phenotypic/genotypic correlation.
August 1992, The New Zealand medical journal,
K H Fischbeck, and D L Schotland
[X-linked muscular dystrophy: is prevention possible?].
January 1990, Pediatrie,
K H Fischbeck, and D L Schotland
Genetic counselling in X-linked muscular dystrophy.
January 1969, Journal of the neurological sciences,
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