Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

1986 • 3,231 citations

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1990 • 1,882 citations

High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones

1990 • 1,357 citations

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1990 • 1,300 citations

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1991 • 944 citations

The candidate Wilms' tumour gene is involved in genitourinary development

1990 • 884 citations

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

1991 • 850 citations

Immunological method for mapping genes on Drosophila polytene chromosomes.

1982 • 772 citations

Association of Wilms's Tumor with Aniridia, Hemihypertrophy and Other Congenital Malformations

1964 • 603 citations

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

1991 • 471 citations

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

1979 • 404 citations

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11

1988 • 252 citations

Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

1987 • 220 citations

Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study.

1988 • 217 citations

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

1988 • 215 citations

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

1990 • 213 citations

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

1991 • 169 citations

A Mouse Model of the Aniridia-Wilms Tumor Deletion Syndrome

1990 • 136 citations

High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

1992 • 131 citations

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.

1985 • 122 citations

The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus

1986 • 118 citations

Wilms' tumour: reconciling genetics and biology

1992 • 107 citations

Role for the Wilms tumor gene in genital development?

1990 • 94 citations

Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11

1988 • 91 citations

Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor

1983 • 81 citations

Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor

1988 • 78 citations

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

1990 • 76 citations

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

1987 • 72 citations

A deletion map of the WAGR region on chromosome 11.

1989 • 59 citations

Two Anonymous DNA Segments Distinguish the Wilms' Tumor and Aniridia Loci

1988 • 59 citations

Cloning of Breakpoints of a Chromosome Translocation Identifies the AN2 Locus

1989 • 53 citations

Parental origin of de novo constitutional deletions of chromosomal band 11p13.

1990 • 51 citations

Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare

1991 • 43 citations

Heritable Fraction of Unilateral Wilms Tumor

1988 • 32 citations

Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers

1988 • 30 citations

Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids

1988 • 28 citations

CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia

1989 • 22 citations

The distal region of 11p13 and associated genetic diseases

1991 • 21 citations

Chromosomal assignment of seven human genomic DNA sequences associated with restriction fragment length polymorphisms

1986 • 15 citations