Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophy in cDNA

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1987 • 2,353 citations

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1986 • 1,033 citations

SYSTEMIC GLUTATHIONE DEFICIENCY IN SYMPTOM-FREE HIV-SEROPOSITIVE INDIVIDUALS

1989 • 725 citations

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

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

1984 • 411 citations

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

1985 • 390 citations

PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

1985 • 380 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

A strategy to reveal high-frequency RFLPs along the human X chromosome.

1984 • 361 citations

RADIOTHERAPY AND HYPERBARIC OXYGEN IN HEAD AND NECK CANCER

1977 • 321 citations

A cDNA clone from the Duchenne/Becker muscular dystrophy gene

1987 • 261 citations

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1985 • 217 citations

Germline mosaicism and Duchenne muscular dystrophy mutations

1987 • 199 citations

Population incidence and segregation ratios in the Martin‐Bell syndrome

1986 • 186 citations

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

1981 • 147 citations

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1987 • 133 citations

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male

1987 • 123 citations

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1984 • 119 citations

Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

1985 • 86 citations

Prenatal Diagnosis and Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy

1987 • 75 citations

An (X;11) translocation in a girl with Duchenne muscular dystrophy

1980 • 67 citations

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker

1987 • 65 citations

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

1986 • 62 citations

EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY

1987 • 53 citations

DNA analysis of first-trimester chorionic villous biopsies: test for maternal contamination.

1984 • 27 citations

Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy

1986 • 18 citations