Found: 40
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Four Years Analysis of Cancer Genetic Clinics Activity in France from 1994 to 1997: A Survey on 801 Patients.
- Published in:
- Disease Markers, 1999, v. 15, n. 1-3, p. 15
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- Publication type:
- Article
Novel BRCA2 pathogenic variant c.5219 T > G; p.(Leu1740Ter) in a consanguineous Senegalese family with hereditary breast cancer.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0814-y
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- Publication type:
- Article
Physicians' attitudes towards mammography and prophylactic surgery for hereditary breast/ovarian cancer risk and subsequently published guidelines.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 3, p. 204, doi. 10.1038/sj.ejhg.5200418
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- Publication type:
- Article
Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer.
- Published in:
- Prostate, 2021, v. 81, n. 6, p. 318, doi. 10.1002/pros.24109
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- Publication type:
- Article
Response of a KIT-Positive Extra-Abdominal Fibromatosis to Imatinib Mesylate and KIT Genetic Analysis.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2006, v. 98, n. 8, p. 562, doi. 10.1093/jnci/djj137
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- Publication type:
- Article
Re: Gene expression profiles of BRCA1-linked, BRCA2-linked, and sporadic ovarian cancers.
- Published in:
- 2002
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- Publication type:
- commentary
Impact of gene patents on the cost-effective delivery of care: the case of BRCA1 genetic testing.
- Published in:
- 2003
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- Publication type:
- journal article
IMPACT OF GENE PATENTS ON THE COST-EFFECTIVE DELIVERY OF CARE: THE CASE OF BRCA1 GENETIC TESTING.
- Published in:
- International Journal of Technology Assessment in Health Care, 2003, v. 19, n. 2, p. 287, doi. 10.1017/S0266462303000266
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- Publication type:
- Article
Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: differences among English, French, and Canadian women.
- Published in:
- 2001
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- Publication type:
- journal article
Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO).
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 130, n. 3, p. 927, doi. 10.1007/s10549-011-1655-3
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- Publication type:
- Article
Prediction of BRCA1 Germ-Line Mutation Status in Patients with Breast Cancer Using Histoprognosis Grade, MS110, Lys27H3, Vimentin, and KI67.
- Published in:
- Pathobiology, 2013, v. 80, n. 5, p. 219, doi. 10.1159/000339432
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- Publication type:
- Article
Re: familial multiple myeloma: a family study and review of the literature.
- Published in:
- 2002
- By:
- Publication type:
- commentary
Re: Biologic characteristics of interval and screen-detected breast cancers.
- Published in:
- 2000
- By:
- Publication type:
- letter
Histological type and syncytial growth pattern affect E-cadherin expression in a multifactorial analysis of a combined panel of sporadic and BRCA1-associated breast cancers.
- Published in:
- International Journal of Cancer, 1999, v. 83, n. 1, p. 45, doi. 10.1002/(SICI)1097-0215(19990924)83:1<45::AID-IJC9>3.0.CO;2-G
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- Publication type:
- Article
Novel indications for BRCA1 screening using individual clinical and morphological features.
- Published in:
- International Journal of Cancer, 1999, v. 84, n. 3, p. 263, doi. 10.1002/(SICI)1097-0215(19990621)84:3<263::AID-IJC11>3.0.CO;2-G
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- Publication type:
- Article
Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas.
- Published in:
- International Journal of Cancer, 1998, v. 75, n. 2, p. 181, doi. 10.1002/(SICI)1097-0215(19980119)75:2<181::AID-IJC3>3.0.CO;2-Q
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- Publication type:
- Article
Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104302
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- Publication type:
- Article
Case-Control Cohort Study of Patients' Perceptions of Disability in Mastocytosis.
- Published in:
- PLoS ONE, 2008, v. 3, n. 5, p. 1, doi. 10.1371/journal.pone.0002266
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- Publication type:
- Article
Phenotypic and Genotypic Characteristics of Mastocytosis According to the Age of Onset.
- Published in:
- PLoS ONE, 2008, v. 3, n. 4, p. 1, doi. 10.1371/journal.pone.0001906
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- Publication type:
- Article
Steroid receptors in hereditary breast carcinomas associated with BRCA1 or BRCA2 mutations or unknown susceptibility genes.
- Published in:
- 1999
- By:
- Publication type:
- commentary
GATA2 gene analysis in several forms of hematological malignancies including familial aggregations.
- Published in:
- 2017
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- Publication type:
- journal article
Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies.
- Published in:
- 2016
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- Publication type:
- journal article
BARD1 homozygous deletion, a possible alternative to BRCA1 mutation in basal breast cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 12, p. 1143, doi. 10.1002/gcc.20822
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- Publication type:
- Article
Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines.
- Published in:
- Genes, Chromosomes & Cancer, 2002, v. 33, n. 2, p. 217, doi. 10.1002/gcc.10022
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- Publication type:
- Article
Patterns of loss of heterozygosity at loci from chromosome arm 13q suggest a possible involvement of BRCA2 in sporadic breast tumors.
- Published in:
- Genes, Chromosomes & Cancer, 1995, v. 13, n. 4, p. 291, doi. 10.1002/gcc.2870130410
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- Publication type:
- Article
GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers.
- Published in:
- Frontiers in Oncology, 2018, p. 1, doi. 10.3389/fonc.2018.00490
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- Publication type:
- Article
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 153, doi. 10.1007/s10689-016-9931-3
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- Publication type:
- Article
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 4, p. 497, doi. 10.1007/s10689-016-9873-9
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- Publication type:
- Article
Behavioral and Economic Impact of a Familial History of Cancers.
- Published in:
- Familial Cancer, 2005, v. 4, n. 4, p. 307, doi. 10.1007/s10689-005-3143-6
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- Publication type:
- Article
Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome.
- Published in:
- Human Mutation, 2009, v. 30, n. 6, p. 867, doi. 10.1002/humu.20947
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- Publication type:
- Article
Three novel BRCA2 germline mutations (1864 delT, 6132 del4, 8208 del5) detected in breast cancer families identified in the south of France.
- Published in:
- Human Mutation, 2001, v. 17, n. 2, p. 155, doi. 10.1002/1098-1004(200102)17:2<155::AID-HUMU14>3.0.CO;2-F
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- Publication type:
- Article
Three novel BRCA1 germline mutations (1104delAA, 1276delTT, 3747delGA) detected in breast/ovarian cancer families identified in the south of France.
- Published in:
- Human Mutation, 2001, v. 17, n. 2, p. 154, doi. 10.1002/1098-1004(200102)17:2<154::AID-HUMU13>3.0.CO;2-L
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- Publication type:
- Article
A novel germline in frame deletion (4128del3) of the BRCA2 gene detected in a breast/ovarian cancer family with fallopian tube and brain tumors identified in the north of France.
- Published in:
- Human Mutation, 2001, v. 17, n. 2, p. 155, doi. 10.1002/1098-1004(200102)17:2<155::AID-HUMU15>3.0.CO;2-C
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- Publication type:
- Article
Evidence for an ancient BRCA1 pathogenic variant in inherited breast cancer patients from Senegal.
- Published in:
- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41525-020-0114-7
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- Publication type:
- Article
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions.
- Published in:
- Oncogene, 1997, v. 14, n. 3, p. 339, doi. 10.1038/sj.onc.1200818
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- Publication type:
- Article
SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis.
- Published in:
- BMC Neurology, 2011, v. 11, n. 1, p. 9, doi. 10.1186/1471-2377-11-9
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- Publication type:
- Article
Moesin expression is a marker of basal breast carcinomas.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 8, p. 1779, doi. 10.1002/ijc.22923
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- Publication type:
- Article
Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 2, p. 230, doi. 10.1002/ijc.21176
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- Publication type:
- Article
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Patients’ characteristics and rate of Internet use to obtain cancer information.
- Published in:
- Journal of Public Health, 2006, v. 28, n. 3, p. 235, doi. 10.1093/pubmed/fdl019
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- Publication type:
- Article