Three non‐overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1984 • 4,899 citations

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

1990 • 1,882 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

Alternative splicing and genomic structure of the Wilms tumor gene WT1.

1991 • 628 citations

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1985 • 555 citations

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

1991 • 471 citations

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1989 • 448 citations

Reduction to Homozygosity of Genes on Chromosome 11 in Human Breast Neoplasia

1987 • 329 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential

1980 • 295 citations

Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome

1983 • 289 citations

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1987 • 273 citations

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting.

1989 • 260 citations

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

1988 • 252 citations

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

1988 • 215 citations

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.

1989 • 206 citations

A third Wilms' tumor locus on chromosome 16q.

1992 • 201 citations

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1988 • 192 citations

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1992 • 191 citations

Zinc finger point mutations within the WT1 gene in Wilms tumor patients.

1992 • 159 citations

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

1989 • 147 citations

Chromosome analysis of 31 Wilms' tumors.

1990 • 131 citations

Suppression of Tumorigenicity in Wilms Tumor by the p15.5-p14 Region of Chromosome 11

1991 • 124 citations

A Comprehensive and Critical Assessment of Overgrowth and Overgrowth Syndromes

1989 • 116 citations

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

1992 • 112 citations

Beckwith-wiedemann syndrome, tumourigenesis and imprinting

1992 • 105 citations

Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.

1991 • 103 citations

Report of the committee on the genetic constitution of chromosome 11

1990 • 98 citations

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

1990 • 93 citations

Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level

1988 • 82 citations

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.

1990 • 82 citations

Structural rearrangements of the WT1 gene in Wilms' tumour cells.

1991 • 69 citations

Familial predisposition to wilms tumor does not segregate with the WT1 gene

1991 • 64 citations

Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome

1988 • 62 citations

Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient.

1992 • 60 citations

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

1991 • 43 citations

Report of the committee on the genetic constitution of chromosome 11

1991 • 35 citations

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome

1988 • 34 citations

Report of the Second Chromosome 11 Workshop

1992 • 18 citations

Allelic loss on chromosome 11p is a less frequent event in bilateral than in unilateral Wilms' tumours

1992 • 17 citations

The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15

1992 • 8 citations

Sacl polymorphism in the RRM1 gene

1990 • 7 citations