Поисковый запрос: (<.>A=Devilee, Peter$<.>) |
Общее количество найденных документов : 22
Показаны документы с 1 по 20
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1.
| A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCAI // Genes, Chromosomes and Cancer, 2000. Vol. 27, N 3.-С.295-302
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2.
| Allelotype analysis of flow-sorted breast cancer cells demonstrates genetically related diploid and aneuploid subpopulations in primary tumors and lymph node metastases // Genes, Chromosomes and Cancer, 2000. Vol. 28, N 2.-С.173-183
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3.
| Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testing // Int. J. Cancer, 2002. Vol. 97, N 4.-С.466-471
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4.
| At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma // Genomics, 1989. Vol. 5, N 3.-С.554-560
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5.
| Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer // Genes, Chromosomes and Cancer, 2010. Vol. 49, N 6.-С.539-548
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| Consortium study on 1280 breast carcinomas: Allelic loss on chromosome 17. Targets subregions associated with family history and clinical parameters // Cancer Res., 1998. Vol. 58, N 5.-С.1004-1012
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7.
| Consortium study on 1280 breast carcinomas: Allelic loss on chromosome 17. Targets subregions associated with family history and clinical parameters // Cancer Res., 1998. Vol. 58, N 5.-С.1004-1012
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8.
| Consortium study on 1280 breast carcinomas: Allelic loss on chromosome 17. Targets subregions associated with family history and clinical parameters // Cancer Res., 1998. Vol. 58, N 5.-С.1004-1012
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9.
| Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosomespecific repetitive DNA probes // Cancer Res., 1988. Vol. 48, N 20.-С.5825-5830
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| Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma // Cancer Res., 1991. Vol. 51, N 3.-С.1020-1025
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| Genetic heterogeneity of breast-ovarian cancer revisited // Amer. J. Hum. Genet., 1995. Vol. 57, N 4.-С.957-958
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12.
| Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: Results of an international study // Amer. J. Hum. Genet., 1998. Vol. 62, N 6.-С.1381--1388
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13.
| Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic loss // Proc. Nat. Acad. Sci. USA, 1996. Vol. 93, N 17.-С.9172-9176
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14.
| Mutant BRCA1 alleles transmission: Different approaches and different biases // Int. J. Cancer, 2004. Vol. 113, N 1.-С.166-167
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15.
| Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma // J. Pathol., 1999. Vol. 189, N 4.-С.504-513
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| Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma // J. Pathol., 1999. Vol. 189, N 4.-С.504-513
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17.
| Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma // J. Pathol., 1999. Vol. 189, N 4.-С.504-513
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18.
| Mutations in SDHD, a mitochondrial complex II gene, in hereditry paraganglioma // Science, 2000. Vol. 287, N 5454.-С.848-851
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19.
| Serrated adenomas and mixed polyposis caused by a splice acceptor deletion in the mouse Smad4 gene // Genes, Chromosomes and Cancer, 2003. Vol. 36, N 3.-С.273-282
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20.
| Devilee Somatic genetic changes in human breast cancer // Biochim. et biophys. acta. Rev. Cancer, 1994. Vol. 1198, N 2-3.-С.113-130
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