A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome
Data up to Jan 2025
Total Citations Per Year
Abstract
References (52)
Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectors
1985 • 15,222 citations
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
1980 • 8,270 citations
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
1986 • 2,968 citations
Lambda replacement vectors carrying polylinker sequences
1983 • 1,809 citations
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
1977 • 1,372 citations
Forensic application of DNA ‘fingerprints’
1985 • 1,163 citations
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
1988 • 1,140 citations
Isolation of a transforming sequence from a human bladder carcinoma cell line
1982 • 776 citations
Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion
1978 • 726 citations
Constitutive Fragile Sites and Cancer
1984 • 693 citations
The "beta-like-globin" gene domain in human erythroid cells.
1985 • 634 citations
Mutation and Cancer: A Model for Wilms' Tumor of the Kidney<xref ref-type="fn" rid="FN2">2</xref>
1972 • 623 citations
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA
1984 • 586 citations
DNA polymerase ? inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
1984 • 581 citations
Spontaneous Mutation in Man
1975 • 346 citations
Clustering of hypervariable minisatellites in the proterminal regions of human autosomes
1988 • 292 citations
Report of the committee on human gene mapping by recombinant DNA techniques
1984 • 274 citations
Genetics of Wilms' tumor
1981 • 216 citations
Epidemiological Features of Wilms' Tumor: Results of the National Wilms' Tumor Study<xref ref-type="fn" rid="fn2">2</xref>
1982 • 213 citations
Isolation and characterization of the human catalase gene
1986 • 212 citations
Nucleotide sequence of the human parathyroid hormone gene.
1983 • 206 citations
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
1988 • 154 citations
A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination
1987 • 154 citations
Report of the committee on the genetic constitution of chromosomes 10, 11, and 12
1987 • 146 citations
DNA Sequence and Regional Assignment of the Human Follicle-Stimulating Hormone β-Subunit Gene to the Short Arm of Human Chromosome 11
1987 • 131 citations
A cluster of chromosome 11p13 translocations found via distinct D-D and D-D-J rearrangements of the human T cell receptor delta chain gene.
1988 • 127 citations
A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids
1989 • 126 citations
Genetics of somatic mammalian cells: genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes.
1976 • 120 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
Epidemiological Features of Wilms’ Tumor: Results of the National Wilms’ Tumor Study
1982 • 103 citations
Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes
1988 • 97 citations
Breakpoints in the human T-cell antigen receptor α-chain locus in two T-cell leukaemia patients with chromosomal translocations
1985 • 93 citations
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.
1985 • 93 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
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
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster
1988 • 69 citations
Implications of fragile X expression in normal males for the nature of the mutation
1986 • 62 citations
Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences.
1982 • 57 citations
Molecular cytogenetics: toward dissection of the contiguous gene syndromes.
1988 • 56 citations
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]
1986 • 53 citations
Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 1 of 9)
1987 • 52 citations
Parental origin of de novo constitutional deletions of chromosomal band 11p13.
1990 • 51 citations
Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms
1986 • 51 citations
The human calcitonin gene is located on the short ARM of chromosome 11
1984 • 42 citations
A pedigree of aniridia with a discussion of germinal mosaicism in man.
1955 • 34 citations
The T-cell receptor delta chain locus is disrupted in the T-ALL associated t(11;14)(p13;q11) translocation
1989 • 28 citations
Wilms tumor in five cousins.
1980 • 19 citations
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1?p13 deletion associated with the AGR syndrome
1988 • 15 citations
Wilms Tumor in Five Cousins
1980 • 15 citations
Localization of the LDHA gene to 11p14?11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13
1986 • 12 citations
Mapping of Human Chromosome 11: Organization of Genes within the Wilms' Tumor Region of the Chromosome
1986 • 5 citations