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

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

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

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

1984 • 361 citations

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

1984 • 279 citations

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

1980 • 238 citations

Sequence of the promoter region of the gene for human X-linked 3-phosphoglycerate kinase

1984 • 203 citations

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

1984 • 146 citations

Tenth International Workshop on Human Gene Mapping

1988 • 143 citations

Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus

1985 • 127 citations

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.

1986 • 127 citations

X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect

1989 • 94 citations

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

1987 • 77 citations

Multi-allelic RFLP for M27β, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]

1987 • 69 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

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

1988 • 56 citations

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

1989 • 47 citations

Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11

1988 • 32 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

Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27? (DXS255)

1989 • 18 citations

A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12

1987 • 12 citations

RFLP detected by an X-Uinked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)

1986 • 12 citations

An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146)

1986 • 9 citations