Frame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia

1985 • 9,128 citations

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1987 • 5,139 citations

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

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1987 • 2,333 citations

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1988 • 1,501 citations

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1988 • 1,140 citations

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

1986 • 1,033 citations

Disorders of Voluntary Muscle

1965 • 576 citations

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

1986 • 468 citations

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1983 • 394 citations

Selection of initiation sites by eucaryotic ribosomes: effect of inserting AUG triplets upstream from the coding sequence for preproinsulin

1984 • 390 citations

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

1985 • 390 citations

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

1985 • 368 citations

Clinical investigation in duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history

1983 • 354 citations

A method to detect and characterize point mutations in transcribed genes: amplification and overexpression of the mutant c-Ki-ras allele in human tumor cells.

1985 • 320 citations

A cDNA clone from the Duchenne/Becker muscular dystrophy gene

1987 • 261 citations

Initiation of translation at internal AUG codons in mammalian cells

1984 • 231 citations

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1987 • 201 citations

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

1987 • 192 citations

Effect of upstream reading frames on translation efficiency in simian virus 40 recombinants.

1986 • 125 citations

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

1984 • 121 citations

Partial gene duplication in Duchenne and Becker muscular dystrophies.

1988 • 74 citations

A cosmid vector that facilitates restriction enzyme mapping.

1985 • 56 citations

A comparison between mammalian and avian fast skeletal muscle alkali myosin light chain genes: regulatory implications

1985 • 50 citations

A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region

1987 • 39 citations

Population data on benign and severe forms of X-linked muscular dystrophy

1987 • 37 citations

Relation between height and clinical course in Duchenne muscular dystrophy

1988 • 29 citations

Microdeletions in patients with X‐linked muscular dystrophy: molecular‐clinical correlations

1988 • 19 citations

Genetic heterogeneity in Duchenne Dystrophy

1987 • 11 citations