Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Molecular Cloning. A Laboratory Manual

1983 • 27,328 citations

PCR protocols — A guide to methods and applications

1990 • 12,897 citations

Dystrophin: The protein product of the duchenne muscular dystrophy locus

1987 • 4,477 citations

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

1988 • 1,501 citations

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes.

1981 • 1,165 citations

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

1989 • 940 citations

Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface

1988 • 617 citations

Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

1988 • 563 citations

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

1989 • 498 citations

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

1984 • 411 citations

Cytogenetic Analysis by In Situ Hybridization with Fluorescently Labeled Nucleic Acid Probes

1986 • 287 citations

Multiple fluorescence in situ hybridization

1990 • 267 citations

Rapid detection of human chromosome 21 aberrations by in situ hybridization.

1988 • 251 citations

MULTIPLEX PCR FOR THE DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY

1990 • 231 citations

Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

1987 • 220 citations

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

1989 • 203 citations

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.

1989 • 155 citations

Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.

1988 • 154 citations

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

1990 • 153 citations

Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome.

1982 • 140 citations

A deletion hot spot in the Duchenne muscular dystrophy gene

1988 • 114 citations

Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes

1989 • 72 citations

Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridization

1986 • 63 citations

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

1986 • 62 citations

Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.

1978 • 60 citations

High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridization

1989 • 60 citations

Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8

1989 • 37 citations

Dystrophin immunocytochemistry in muscle culture: Detection of a carrier of Duchenne muscular dystrophy

1989 • 26 citations

Duchenne muscular dystrophy: the gene and the protein.

1989 • 25 citations

The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.

1988 • 15 citations

DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening

1989 • 12 citations