Showing results (151-160 of 473) with videos related to

Sort By:
Pageof 48
Hereditary Cancer in Clinical Practice|March 18, 2010
Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical managementLiesbeth Hameetman, Judith Vmg Bovée, Antonie Hm Taminiau, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Economic and Practical Factors in Diagnosing HNPCC Using Clinical Criteria, Immunohistochemistry and Microsatellite Instability AnalysisFrancesca Pigatto, Adrian Bateman, David Bunyan, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Supernormal electro-oculograms in patients with neurofibromatosis type 1Wojciech Lubiński, Stanisław Zajaczek, Zbigniew Sych, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Intronic TP53 Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer FamiliesXuan Liu, Hans-Peter Sinn, Hans Ulrich Ulmer, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Colorectal tumour microsatellite instability test results: perspectives from patientsNoralane M Lindor, Jeff Sloan, Richard Goldberg, et al.
Hereditary Cancer in Clinical Practice|April 2, 2021
Should the BCRA1/2-mutations healthy carriers be valid candidates for hematopoietic stem cell donation?Alberto Fresa, Simona Sica
Hereditary Cancer in Clinical Practice|March 21, 2013
Should extragonadal germ cell tumors be included in studies of families with testicular germ cell tumors?Rodrigo Santa Cruz Guindalini, Edite Paulo de Oliveira, Marina Cavalcanto Moroja Silvino, et al.
Hereditary Cancer in Clinical Practice|November 22, 2012
Chemokine Ligand 5 (CCL5) and chemokine receptor (CCR5) genetic variants and prostate cancer risk among men of African Descent: a case-control studyLacreis R Kidd, Dominique Z Jones, Erica N Rogers, et al.
Hereditary Cancer in Clinical Practice|August 15, 2013
Comparison of whole genome amplification and nested-PCR methods for preimplantation genetic diagnosis for BRCA1 gene mutation on unfertilized oocytes-a pilot studyDanuta Michalska, Kinga Jaguszewska, Joanna Liss, et al.
Hereditary Cancer in Clinical Practice|January 12, 2012
Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancersRamunas Janavicius, Pavel Elsakov
Pageof 48