Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

1980 • 8,270 citations

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

1977 • 1,372 citations

The Genetics of Human Populations

1972 • 1,252 citations

The Primary Immunodeficiencies

1984 • 1,111 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

X-Linked Agammaglobulinemia

1985 • 415 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

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

1984 • 361 citations

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1982 • 334 citations

The Primary Immunodeficiencies

1984 • 288 citations

Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase

1984 • 279 citations

B Lymphocyte Precursors in Human Bone Marrow: An Analysis of Normal Individuals and Patients with Antibody-Deficiency States

1978 • 236 citations

Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase.

1983 • 232 citations

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

1982 • 191 citations

Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X Chromosome

1984 • 188 citations

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.

1982 • 182 citations

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

1984 • 178 citations

Identification and Characterization of Subpopulations of Lymphocytes in Human Peripheral Blood after Fractionation on Discontinuous Gradients of Albumin THE CELLULAR DEFECT IN X-LINKED AGAMMAGLOBULINEMIA

1973 • 144 citations

Primary immunodeficiency diseases

1983 • 141 citations

X-Linked Agammaglobulinemia

2000 • 120 citations

Interstitial deletion in the ?critical region? of the long arm of the X chromosome in a mentally retarded boy and his normal mother

1983 • 57 citations

An RFLP detecting single copy X-chromosome fragment, dlc56, from Xp22-Xpter [HGM8 assignment no.DXS 143]

1985 • 54 citations

Linkage Analysis in Man

1980 • 52 citations

Inherited interstitial del(Xp) with minimal clinical consequences: With a note on the location of genes controlling phenotypic features

1979 • 40 citations

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

1985 • 38 citations

Defective B cell function associated with inherited interstitial deletion of the short arm of the X chromosome.

1983 • 19 citations

Immunodeficiency associated with a deletion in the short arm of the X-chromosome.

1981 • 13 citations