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

Data up to Jan 2025

Published1987
Citations192
References17

Total Citations Per Year

Abstract

References (17)

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

Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric Field

1986 • 920 citations

Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis

1984 • 887 citations

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

1986 • 468 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

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

1985 • 368 citations

A cDNA clone from the Duchenne/Becker muscular dystrophy gene

1987 • 261 citations

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

1987 • 171 citations

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

1986 • 152 citations

Athymic mice express a high level of functional γ-chain but greatly reduced levels of α- and β-chain T-cell receptor messages

1986 • 133 citations

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1987 • 133 citations

Long-range restriction map around the Duchenne muscular dystrophy gene

1986 • 120 citations

A giant locus for the Duchenne and Becker muscular dystrophy gene

1987 • 88 citations

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

1986 • 62 citations

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Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field… (1987) – Nature | Metascience Observatory Explorer