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Human Genetics|June 4, 2005
SNP microarray analysis for genome-wide detection of crossover regionsMichael Wirtenberger, Kari Hemminki, Bowang Chen, et al.BMC Genomics|March 21, 2007
Allelotyping of pooled DNA with 250 K SNP microarraysStefan Wilkening, Bowang Chen, Michael Wirtenberger, et al.American Journal of Medical Genetics. Part A|July 14, 2006
Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphomaIngo Helbig, Michael Wirtenberger, Anna Jauch, et al.American Journal of Medical Genetics. Part A|August 2, 2005
Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive traitChristian Tiemann, Christoph Bührer, Barbara Burwinkel, et al.Carcinogenesis|November 20, 2004
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer riskBernd Frank, Kari Hemminki, Michael Wirtenberger, et al.Cancer Letters|June 10, 2006
Aurora kinases A and B and familial breast cancer riskSandrine Tchatchou, Michael Wirtenberger, Kari Hemminki, et al.Carcinogenesis|October 20, 2005
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancerMichael Wirtenberger, Sandrine Tchatchou, Kari Hemminki, et al.Carcinogenesis|September 8, 2006
The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancerMichael Wirtenberger, Julia Schmutzhard, Kari Hemminki, et al.Carcinogenesis|February 28, 2006
Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancerMichael Wirtenberger, Bernd Frank, Kari Hemminki, et al.International Journal of Cancer|June 2, 2005
c-MYC Asn11Ser is associated with increased risk for familial breast cancerMichael Wirtenberger, Kari Hemminki, Asta Försti, et al.Pageof 2