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Separation of random fragments of DNA according to properties of their sequences.
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4420-4
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DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory.
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Risk factors for breast cancer in women with proliferative breast disease.
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Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis.
Nucleic Acids Res. 1985 May 10;13(9):3111-29
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Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis.
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Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.
Proc Natl Acad Sci U S A. 1989 Jan;86(1):232-6
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Histopathologic risk factors for breast cancer in women with benign breast disease.
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Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers.
Proc Natl Acad Sci U S A. 1989 Dec;86(23):9389-93
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Evidence implicating at least two genes on chromosome 17p in breast carcinogenesis.
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Characterization of chromosomal anomalies in human breast cancer. A comparison of 30 paradiploid cases with few chromosome changes.
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Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer.
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Allelic loss on a chromosome 17 in ductal carcinoma in situ of the breast.
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Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors.
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Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted.
Cancer Res. 1993 Dec 1;53(23):5617-9
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Patterns of allele losses suggest the existence of five distinct regions of LOH on chromosome 17 in breast cancer.
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Molecular genetic studies of early breast cancer evolution.
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Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p and 17q.
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Comparative allelotype of in situ and invasive human breast cancer: high frequency of microsatellite instability in lobular breast carcinomas.
Cancer Res. 1995 Sep 15;55(18):3976-81
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Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors.
Oncology. 1995 Nov-Dec;52(6):448-53
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Allelic loss and the progression of breast cancer.
Cancer Res. 1995 Nov 15;55(22):5180-3
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Multiplex genotype determination at a large number of gene loci.
Proc Natl Acad Sci U S A. 1996 Mar 19;93(6):2582-7
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Papillary apocrine change of the breast: associations with atypical hyperplasia and risk of breast cancer.
Cancer Epidemiol Biomarkers Prev. 1996 Jan;5(1):29-32
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Lobular neoplasia. Long term risk of breast cancer and relation to other factors.
Cancer. 1996 Sep 1;78(5):1024-34
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Loss of heterozygosity in normal tissue adjacent to breast carcinomas.
Science. 1996 Dec 20;274(5295):2057-9
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Deletion map of chromosome 16q in ductal carcinoma in situ of the breast: refining a putative tumor suppressor gene region.
Cancer Res. 1996 Dec 15;56(24):5605-9
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Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.
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Genetic changes in intraductal breast cancer detected by comparative genomic hybridization.
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Genetic heterogeneity and clonal evolution underlying development of asynchronous metastasis in human breast cancer.
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Identical clonality of both components of mammary carcinosarcoma with differential loss of heterozygosity.
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Discriminating between allelic and interlocus differences among human immunoglobulin VH4 sequences by analyzing single spermatozoa.
Hum Genet. 1997 Jul;100(1):96-100
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Microsatellite instability and loss of heterozygosity in mammary carcinoma and its probable precursors.
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Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters.
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Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci.
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Cytogenetic features of twenty-six primary breast cancers.
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Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q.
Oncogene. 1991 Sep;6(9):1705-11
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Accumulation of genetic alterations and progression of primary breast cancer.
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Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss.
Int J Cancer. 1992 Feb 20;50(4):544-8
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Heterogeneity for allelic loss in human breast cancer.
J Natl Cancer Inst. 1992 Apr 1;84(7):506-10
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Genetic alterations of the tumour suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas.
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Indicators of increased breast cancer risk in humans.
J Cell Biochem Suppl. 1992;16G:175-82
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Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.
Oncogene. 1993 Mar;8(3):781-5
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Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas.
Hum Genet. 1993 Mar;91(1):6-12
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Prognostic significance of benign proliferative breast disease.
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