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Votre recherche : [La BTT] MOT CLE égal Génétique
132 résultat(s)

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Borsting C, Mikkelsen M, Morling N. Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory. Transfus Med Hemother. 2012;39:195-201.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Borsting C, Morling N. Reinvestigations of six unusual paternity cases by typing of autosomal single-nucleotide polymorphisms. Transfusion. 2012;52:425-430.
Thèmes : Génétique ; maj-2012-11

Bugert P, Rink G, Kemp K, Kluter H. Blood Group ABO Genotyping in Paternity Testing. Transfus Med Hemother. 2012;39:182-186.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Bugert P, Kluter H. 100 Years after von Dungern & Hirschfeld: Kinship Investigation from Blood Groups to SNPs. Transfus Med Hemother. 2012;39:161-162.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Fayrouz IN, Farida N, Irshad AH. Relation between fingerprints and different blood groups. J Forensic Leg Med. 2012;19:18-21.
Thèmes : Systèmes de groupes sanguins ; Génétique ; maj-2012-11

Geserick G, Wirth I. Genetic Kinship Investigation from Blood Groups to DNA Markers. Transfus Med Hemother. 2012;39:163-175.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Pena HB, Pena SD. Automated Genotyping of a Highly Informative Panel of 40 Short Insertion-Deletion Polymorphisms Resolved in Polyacrylamide Gels for Forensic Identification and Kinship Analysis. Transfus Med Hemother. 2012;39:211-216.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Phillips C, Garcia-Magarinos M, Salas A, Carracedo A, Lareu MV. SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests? Transfus Med Hemother. 2012;39:202-210.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Schneider PM. Beyond STRs: The Role of Diallelic Markers in Forensic Genetics. Transfus Med Hemother. 2012;39:176-180.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Schwark T, Meyer P, Harder M, Modrow JH, von Wurmb-Schwark N. The SNPforID Assay as a Supplementary Method in Kinship and Trace Analysis. Transfus Med Hemother. 2012;39:187-193.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2012-11

Sirolli V, Rossi C, Di Castelnuovo A, Felaco P, Amoroso L, Zucchelli M, Ciavardelli D, Di Ilio C, Sacchetta P, Bernardini S, Arduini A, Bonomini M, Urbani A. Toward personalized hemodialysis by low molecular weight amino-containing compounds: future perspective of patient metabolic fingerprint. Blood Transfus. 2012;10:s78-s88.
Thèmes : Génétique ; maj-2012-11

Chahal SM, Virk RK, Kaur S, Bansal R. Social stratification in the Sikh population of Punjab (India) has a genetic basis: evidence from serological and biochemical markers. Genet Test Mol Biomarkers. 2011;15:543-556.
Thèmes : Génétique ; maj-2012-09

Charron D. HLA, immunogenetics, pharmacogenetics and personalized medicine. Vox Sang. 2011;100:163-166.
Thèmes : HLA et systèmes leucocytaires ; Histoire - Economie - Prospective ; Génétique ; maj-2011-11

Condel K, Salih MA. A simple method for establishing concordance between short-tandem-repeat allele frequency databases. Transfusion. 2011;51:986-992.
Thèmes : Génétique ; maj-2011-11

Houston BL, Zelinski T, Israels SJ, Coghlan G, Chodirker BN, Gallagher PG, Houston DS, Zarychanski R. Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred. Blood Cells Mol Dis. 2011;47:226-231.
Thèmes : Génétique ; maj-2012-09

Kim DW, Cho D, Yazer MH, Lee HJ, Kim KH, Shin MG, Suh SP, Shin JH, Ryang DW. A novel a subtype allele that demonstrates allelic competition. Ann Clin Lab Sci. 2011;41:282-284.
Thèmes : Génétique ; maj-2012-09

Patnaik SK, Blumenfeld OO. Patterns of human genetic variation inferred from comparative analysis of allelic mutations in blood group antigen genes. Hum Mutat. 2011;32:263-271.
Thèmes : Systèmes de groupes sanguins ; Génétique ; maj-2012-09

Zachary AA, Leffell MS. Response: Good ethics require good science: why transplant programs should not disclose misattributed parentage. Am J Transplant. 2011;11:179-1.
Thèmes : Génétique ; maj-2012-09

Anglicheau D, Muthukumar T, Suthanthiran M. MicroRNAs: small RNAs with big effects. Transplantation. 2010;90:105-112.
Thèmes : Génétique ; maj-2010-11

Feero WG, Guttmacher AE, COLLINS FS. Genomic medicine--an updated primer. N Engl J Med. 2010;362:2001-2011.
Thèmes : Génétique ; maj-2010-11

Hopp K, Weber K, Bellissimo D, Johnson ST, Pietz B. High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform. Transfusion. 2010;50:40-46.
Thèmes : Méthodes en immuno-hématologie ; Génétique ; maj-2010-04

Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med. 2010;363:166-176.
Thèmes : Génétique ; maj-2010-11

Soejima M, Tsuchiya Y, Egashira K, Kawano H, Sagawa K, Koda Y. Development and validation of a SYBR Green I-based real-time polymerase chain reaction method for detection of haptoglobin gene deletion in clinical materials. Transfusion. 2010;50:1322-1327.
Thèmes : Assurance de qualité en transfusion sanguine ; Complications immunologiques ; Génétique ; maj-2010-11

Bienvenu T. L' inactivation du chromosome X. Les maladies génétiques liées au chromosomes X. Biofutur. 2009;n° 304:44-47.
Thèmes : Génétique ; maj-2010-04

Calado RT, Young NS. Telomere diseases. N Engl J Med. 2009;361:2353-2365.
Thèmes : Génétique ; maj-2010-04

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