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Results 1 to 25 of 485

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Misinterpretation of TPMT by a DTC Genetic Testing CompanyBROWNSTEIN, C. A; MARGULIES, D. M; MANZI, S. F et al.Clinical pharmacology and therapeutics. 2014, Vol 95, Num 6, pp 598-600, issn 0009-9236, 3 p.Article

Les tests génétiques grand public en « caméra cachée » = An undercover investigation of DTC testingJORDAN, Bertrand.MS. Médecine sciences. 2011, Vol 27, Num 1, pp 103-106, issn 0767-0974, 4 p.Article

Impact of gene patents on the cost-effective delivery of care: The case of BRCA1 genetic testingSEVILLA, Christine; JULIAN-REYNIER, Claire; EISINGER, Francois et al.International journal of technology assessment in health care. 2003, Vol 19, Num 2, pp 287-300, issn 0266-4623, 14 p.Article

Protection des signatures moléculaires et des tests multigéniques: soyons créatifsCHARPENTIER, Aurélie; CHAJMOWICZ, Marion.Biofutur (Puteaux). 2012, Num 337, pp 58-59, issn 0294-3506, 2 p.Article

The Personal Is Political, the Professional Is Not : Conscientious Objection to Obtaining/Providing/Acting on Genetic InformationFRADER, Joel; BOSK, Charles L.American journal of medical genetics. Part C, Seminars in medical genetics. 2009, Vol 151, Num 1, pp 62-67, issn 1552-4868, 6 p.Conference Paper

Regulatory Issues for Genetic Testing in Clinical PracticeKRISTOFFERSSON, Ulf.Molecular biotechnology. 2008, Vol 40, Num 1, pp 113-117, issn 1073-6085, 5 p.Article

Génomique personnelle : Au carrefour de la science, de l'éthique et de la consommationFRANRENET, Sandra.Biofutur (Puteaux). 2008, Num 292, pp 49-51, issn 0294-3506, 3 p.Article

Maturity-onset diabetes of the young (MODY): how many cases are we missing?SHIELDS, B. M; HICKS, S; SHEPHERD, M. H et al.Diabetologia (Berlin). 2010, Vol 53, Num 12, pp 2504-2508, issn 0012-186X, 5 p.Article

Approaches to the Patient with Neurogenetic DiseaseBIRD, Thomas D.Clinics in laboratory medicine. 2010, Vol 30, Num 4, issn 0272-2712, vii, 785-793 [10 p.]Article

Predictive and Diagnostic Genetic Testing in PsychiatryMITCHELL, Philip B; MEISER, Bettina; WILDE, Alex et al.Clinics in laboratory medicine. 2010, Vol 30, Num 4, issn 0272-2712, viii, 829-846 [19 p.]Article

Genetic Basis of Congenital Upper Limb Anomalies: Analysis of 487 Cases of a Specialized ClinicCARLI, Diana; FAIRPLAY, Tracy; BERNASCONI, Sergio et al.Birth defects research. Clinical and molecular teratology. 2013, Vol 97, Num 12, pp 798-805, issn 1542-0752, 8 p.Article

A rapid genetic counselling and testing in newly diagnosed breast cancer is associated with high rate of risk-reducing mastectomy in BRCA1/2-positive Italian womenCORTESI, L; RAZZABONI, E; FEDERICO, M et al.Annals of oncology. 2014, Vol 25, Num 1, pp 57-63, issn 0923-7534, 7 p.Article

Sensitive Deep-Sequencing-Based HIV-1 Genotyping Assay To Simultaneously Determine Susceptibility to Protease, Reverse Transcriptase, Integrase, and Maturation Inhibitors, as Well as HIV-1 Coreceptor TropismGIBSON, Richard M; MEYER, Ashley M; WINNER, Dane et al.Antimicrobial agents and chemotherapy. 2014, Vol 58, Num 4, pp 2167-2185, issn 0066-4804, 19 p.Article

The performance of BRCA1 immunohistochemistry for detecting germline, somatic, and epigenetic BRCA1 loss in high-grade serous ovarian cancerMEISEL, J. L; HYMAN, D. M; IASONOS, A et al.Annals of oncology. 2014, Vol 25, Num 12, pp 2372-2378, issn 0923-7534, 7 p.Article

Predicting sustained viral response to hepatitis C using a rapid and simple IL28B rs8099917 genotyping assayWEI LI; YANLI ZENG; JUNJIE WANG et al.Antiviral research. 2012, Vol 94, Num 1, pp 54-56, issn 0166-3542, 3 p.Article

Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group StudyFOSTIRA, Florentia; TSITLAIDOU, Marianthi; PAPAKOSTAS, Pavlos et al.Breast cancer research and treatment. 2012, Vol 134, Num 1, pp 353-362, issn 0167-6806, 10 p.Article

Pharmacogenetics of the Antiplatelet Effect of AspirinWÜRTZ, Morten; DALBY KRISTENSEN, Steen; HVAS, Anne-Mette et al.Current pharmaceutical design (Print). 2012, Vol 18, Num 33, pp 5294-5308, issn 1381-6128, 15 p.Article

An Analysis of Pharmaceutical Experience with Decades of Rat Carcinogenicity Testing: Support for a Proposal to Modify Current Regulatory GuidelinesSISTARE, Frank D; MORTON, Daniel; BIENVENU, Jean-Guy et al.Toxicologic pathology. 2011, Vol 39, Num 4, pp 716-744, issn 0192-6233, 29 p.Article

Postgenomics, uncertain futures, and the familiarization of susceptibility genes : Genetics, healthcare, family and kinship in a global perspective: Situated processes of co-constructionCHILIBECK, Gillian; LOCK, Margaret; SEHDEV, Megha et al.Social science & medicine (1982). 2011, Vol 72, Num 11, pp 1768-1775, issn 0277-9536, 8 p.Article

Excellent agreement between genetic and hydrogen breath tests for lactase deficiency and the role of extended symptom assessmentPOHL, D; SAVARINO, E; HERSBERGER, M et al.British journal of nutrition. 2010, Vol 104, Num 6, pp 900-907, issn 0007-1145, 8 p.Article

Public accountability of newborn screening: Collective knowing and decidingWIESER, Bernhard.Social science & medicine (1982). 2010, Vol 70, Num 6, pp 926-933, issn 0277-9536, 8 p.Article

Disparities in BRCA testing: when insurance coverage is not a barrierOLAYA, Windy; ESQUIVEL, Pamela; WONG, Jan H et al.The American journal of surgery. 2009, Vol 198, Num 4, pp 562-565, issn 0002-9610, 4 p.Article

Genetic testing for hereditary cancers : The impact of gender on interest, uptake and ethical considerationsD'AGINCOURT-CANNING, Lori; BAIRD, Patricia.Critical reviews in oncology/hematology. 2006, Vol 58, Num 2, pp 114-123, issn 1040-8428, 10 p.Article

Self-regulation and the behavioural response to DNA risk information : A theoretical analysis and framework for future researchMARTEAU, Theresa M; WEINMAN, John.Social science & medicine (1982). 2006, Vol 62, Num 6, pp 1360-1368, issn 0277-9536, 9 p.Article

Genetic testing for maturity onset diabetes of the young: uptake, attitudes and comparison with hereditary non-polyposis colorectal cancerLILJESTRÖM, B; AKTAN-COLLAN, K; ISOMAA, B et al.Diabetologia (Berlin). 2005, Vol 48, Num 2, pp 242-250, issn 0012-186X, 9 p.Article

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