Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

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

1983 • 26,063 citations

Genomic sequencing.

1984 • 8,343 citations

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

1986 • 2,968 citations

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

1986 • 1,033 citations

The sex-determining region of the human Y chromosome encodes a finger protein

1987 • 847 citations

Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location

1986 • 839 citations

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

1985 • 369 citations

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

1984 • 361 citations

Directional cloning of DNA fragments at a large distance from an initial probe: a circularization method.

1984 • 260 citations

Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis

1987 • 195 citations

Construction and use of human chromosome jumping libraries from NotI-digested DNA

1987 • 145 citations

A highly polymorphic locus in human DNA revealed by cosmid-derived probes.

1985 • 134 citations

[35] Strategies for mapping and cloning macroregions of mammalian genomes

1987 • 112 citations

[6] Double cos site vectors: simplified cosmid cloning

1987 • 112 citations

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes

1989 • 96 citations

Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.

1987 • 85 citations

Construction of aNotI linking library and isolation of new markers close to the Huntington's disease gene

1988 • 75 citations

Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.

1985 • 58 citations

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

1988 • 56 citations

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion

1987 • 53 citations

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

1988 • 53 citations

Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7

1988 • 52 citations

Two different genes for X-linked retinitis pigmentosa

1988 • 43 citations

Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.

1988 • 37 citations

Deletion of the DXS165 locus in patients with classical Choroideremia

1987 • 36 citations

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical‐genealogical evidence

1987 • 34 citations

Choroideremia: further evidence for assignment of the locus to Xq13?Xq21

1986 • 32 citations

Preserving primary cDNA libraries

1987 • 11 citations

Localisation of the endpoints of deletions in the 5′ region of the Duchenne gene using a sequence isolated by chromosome jumping

1988 • 5 citations

Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30 320)

1989 • 2 citations