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Muscular dystrophy in girls with X;autosome translocations

author

Ian W. Craig

published in: Journal of Medical Genetics

date of publication: 1986-12-01

language: English

main subject: muscular dystrophy

Cites articles 39

Date

Title

Authors

1986-04-01

Duchenne muscular dystrophy in a female with a translocation involving Xp21.
1986-12-01

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy
1986-07-01

X;autosome translocations in females with Duchenne or Becker muscular dystrophy
1986-07-01

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

Albert de la Chapelle
1986-01-01

Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monocytic leukemia

Michelle M Le Beau, Janet Rowley
1986-02-01

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy
1985-01-01

High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy
1985-03-01

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome
1985-01-01

Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites

Clara D. Bloomfield
1985-01-01

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.
1985-04-01

Chromatin structure around the c-myc gene in Burkitt lymphomas with upstream and downstream translocation points
1985-12-01

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.
1985-08-01

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

Anthony Monaco
1985-07-01

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

Anthony Monaco
1985-04-01

[Duchenne muscular dystrophy in a female with an X-autosome translocation]
1984-09-01

Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns

Frederick Hecht, Barbara K. Hecht
1984-11-01

Characterization of the human factor VIII gene.
1984-12-01

Constitutive fragile sites and cancer.
1984-01-01

Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation
1984-06-01

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes
1984-11-01

Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus
1983-12-01

Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
1983-01-01

Balanced structural changes involving the human X: effect on sexual phenotype,Balanced structural changes involving the human X: Effect on sexual phenotype
1983-11

High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization

Graeme I. Bell
1983-01-01

High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements
1982-01-01

X-autosome translocations: cytogenetic characteristics and their consequences
1982-05-01

X chromosome in Duchenne muscular dystrophy
1981-12-01

Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus
1981-07-01

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
1981-01-01

Structural anomalies of the X chromosome and inactivation center
1980-05-01

Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis
1980-05-01

Clinical features and classification of the muscular dystrophies

Article - wd:Q33673948

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