Localization of beckwith‐wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5

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

1983 • 26,063 citations

Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients

1990 • 1,471 citations

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

1978 • 1,287 citations

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus

1990 • 1,085 citations

Relaxation of imprinted genes in human cancer

1993 • 792 citations

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1993 • 710 citations

Tumour-suppressor activity of H19 RNA

1993 • 638 citations

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

1989 • 448 citations

Disruption of insulin–like growth factor 2 imprinting in Beckwith–Wiedemann syndrome

1993 • 427 citations

Parental genomic imprinting of the human IGF2 gene

1993 • 422 citations

Monoallelic expression of the human H19 gene

1992 • 409 citations

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1989 • 306 citations

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome

1993 • 290 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

Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome

1983 • 236 citations

Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei.

1991 • 226 citations

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

1992 • 209 citations

Tumor Cell Growth Arrest Caused by Subchromosomal Transferable DNA Fragments from Chromosome 11

1993 • 177 citations

Report of the committee on chromosome and gene loss in human neoplasia

1991 • 158 citations

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases

1984 • 156 citations

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

1990 • 153 citations

A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids

1989 • 126 citations

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

1991 • 124 citations

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma.

1992 • 111 citations

Cloning of cDNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemic cells with 11q23 translocations.

1992 • 110 citations

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

1993 • 97 citations

The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney.

1993 • 95 citations

Fetal rhabdomyomatous nephroblastoma—A variant of Wilms' tumor

1976 • 86 citations

Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

1992 • 76 citations

Malignant rhabdoid tumor: A highly malignant childhood tumor with minimal karyotypic changes

1990 • 75 citations

Molecular analysis of a partial deletion of 22q in a central nervous system rhabdoid tumor

1992 • 72 citations

Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)

1991 • 52 citations

Recurrent Wiedemann‐Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

1992 • 44 citations

Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus.

1989 • 39 citations

A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.

1993 • 37 citations

Mapping of 262 DNA markers into 24 intervals on human chromosome 11.

1992 • 35 citations

Prognostic relevance of DNA content in childhood renal tumours

1989 • 28 citations

Molecular Sublocalization and Characterization of the 11;22 Translocation Breakpoint in a Malignant Rhabdoid Tumor

1994 • 22 citations

An Ordered NotI Fragment Map of Human Chromosome Band 11p15

1994 • 20 citations

Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

1990 • 16 citations

11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis

1992 • 10 citations

Partial trisomy 11p with interatrial septal aneurysm. Case report and literature review.

1985 • 8 citations

Reply to Rivera.

1993 • 1 citations