Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
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Duchenne muscular dystrophy in a female with a translocation involving Xp21.Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyDuchenne muscular dystrophy in one of monozygotic twin girlsMolecular deletion analysis in Duchenne muscular dystrophy.The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy familiesLinkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyDNA analysis in human disease2004 William Allan Award address. Cloning of the DMD gene.On discovery, genomes, the Society, and society.A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.Translocation of the nucleolus organizer region to the human X chromosome.Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessmentGender differences in contractile and passive properties of mdx extensor digitorum longus muscle.Clinical and Genetic Characterization of Female DystrophinopathyHuman X chromosome markers and Duchenne muscular dystrophy.Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.The Duchenne dystrophy story: from phenotype to gene and potential treatment.Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.The molecular genetics of human monogenic diseases.Use of DNA probes for diagnosis and prevention of inherited disorders.An appraisal of the application of recombinant DNA techniques to chromosome defectsRare X chromosome abnormalities in systemic lupus erythematosus and Sjögren's syndrome.Prenatal diagnosis of Duchenne and Becker muscular dystrophy.Turner syndrome and Duchenne muscular dystrophy.What can we learn from assisted bicycle training in a girl with dystrophinopathy? A case study.
P2860
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P2860
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
1984年论文
@zh
1984年论文
@zh-cn
name
Expression of an X-linked musc ...... on of the normal X chromosome.
@ast
Expression of an X-linked musc ...... on of the normal X chromosome.
@en
type
label
Expression of an X-linked musc ...... on of the normal X chromosome.
@ast
Expression of an X-linked musc ...... on of the normal X chromosome.
@en
prefLabel
Expression of an X-linked musc ...... on of the normal X chromosome.
@ast
Expression of an X-linked musc ...... on of the normal X chromosome.
@en
P2093
P356
P1433
P1476
Expression of an X-linked musc ...... on of the normal X chromosome.
@en
P2093
C Verellen-Dumoulin
J Frédéric
M W Thompson
R De Meyer
R G Worton
V D Markovic
P2888
P304
P356
10.1007/BF00270570
P577
1984-01-01T00:00:00Z