The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome.

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

1990 • 597 citations

Chromosome maps of man and mouse. IV

1989 • 219 citations

The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes.

1988 • 180 citations

EXCEPTIONAL INHERITANCE OF A SEX-LINKED GENE IN THE MOUSE EXPLAINED ON THE BASIS THAT THE X/O SEX-CHROMOSOME CONSTITUTION IS FEMALE

1959 • 160 citations

Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome.

1989 • 135 citations

Expression on blood cells of sialophorin, the surface glycoprotein that is defective in Wiskott-Aldrich syndrome

1987 • 134 citations

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

1987 • 77 citations

Conservation and reorganization of loci on the mammalian X chromosome: A molecular framework for the identification of homologous subchromosomal regions in man and mouse

1988 • 65 citations

Multilocus molecular mapping of the mouse X chromosome

1988 • 62 citations

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome

1988 • 60 citations

Genetic control over the inactivation of autosomal genes attached to the X-chromosome

1965 • 60 citations

Enzyme-activity mutations detected in mice after paternal fractionated irradiation

1986 • 31 citations

Wiskott-Aldrich syndrome: new perspectives in pathogenesis and management.

1988 • 23 citations