The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

1974 • 1,022 citations

PEDIGREE DEMONSTRATING A SEX-LINKED RECESSIVE CONDITION CHARACTERIZED BY DRAINING EARS, ECZEMATOID DERMATITIS AND BLOODY DIARRHEA

1954 • 512 citations

Wiskott-Aldrich syndrome

1968 • 422 citations

The Wiskott-Aldrich syndrome in the United States and Canada (1892–1979)

1980 • 238 citations

Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis

1986 • 215 citations

Aberrant O-linked oligosaccharide biosynthesis in lymphocytes and platelets from patients with the Wiskott-Aldrich syndrome.

1991 • 146 citations

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.

1987 • 77 citations

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

1991 • 60 citations

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

1988 • 60 citations

A primary genetic map of the pericentromeric region of the human X chromosome

1988 • 59 citations

Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.

1987 • 48 citations

Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylation

1989 • 47 citations

Investigation of Gyrate Atrophy Using a cDNA Clone for Human Ornithine Aminotransferase

1986 • 45 citations

Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

1987 • 37 citations

The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22

1991 • 37 citations

An 18-locus linkage map of the pericentromeric region of the human X chromosome: Genetic framework for mapping X-linked disorders

1991 • 36 citations

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome

1990 • 29 citations

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction

1989 • 23 citations

A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.

1991 • 20 citations

Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm

1991 • 18 citations