Molecular heterogeneity of translocations associated with muscular dystrophy

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

1986 • 468 citations

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

1985 • 456 citations

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

1985 • 455 citations

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

1985 • 390 citations

Report of the committee on the genetic constitution of the X and Y chromosomes

1985 • 369 citations

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

1985 • 368 citations

An International System for Human Cytogenetic Nomenclature — High-Resolution Banding (1981): ISCN (1981)

1981 • 224 citations

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1984 • 149 citations

Duchenne Muscular Dystrophy Involving Translocation of the dmd Gene Next to Ribosomal RNA Genes

1984 • 128 citations

Muscular dystrophy in girls with X;autosome translocations.

1986 • 127 citations

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1986 • 82 citations

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

1983 • 18 citations