Showing results (1-10 of 125) with videos related to

Sort By:
Pageof 13
Future Oncology (London, England)|April 21, 2012
Germline copy number variations and cancer predispositionAna Cristina Victorino Krepischi, Peter Lees Pearson, Carla Rosenberg
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Structural variation in the human genome: the impact of copy number variants on clinical diagnosisLaia Rodriguez-Revenga, Montserrat Mila, Carla Rosenberg, et al.
Frontiers in Genetics|July 6, 2016
Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer's Disease?Darine Villela, Claudia K Suemoto, Carlos A Pasqualucci, et al.
European Journal of Medical Genetics|March 31, 2015
Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype-phenotype correlationsNatália D Linhares, Marta Svartman, Tatiane C Rodrigues, et al.
Cancer Genetics and Cytogenetics|April 25, 2006
Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell linesKároly Szuhai, Marije Ijszenga, Hans J Tanke, et al.
Stem Cell Research|July 18, 2018
A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblastsUirá Souto Melo, Felipe de Souza Leite, Silvia Costa, et al.
Molecular Genetics and Genomics : MGG|June 5, 2015
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomaliesBruno Faulin Gamba, Antônio Richieri-Costa, Silvia Costa, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 21, 2004
Primary synovial sarcoma of the heart: a cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH of a case with a complex karyotypeHans Martin Hazelbag, Károly Szuhai, Hans J Tanke, et al.
Molecular Syndromology|April 9, 2015
Cleft lip/palate, short stature, and developmental delay in a boy with a 5.6-mb interstitial deletion involving 10p15.3p14Bruno F Gamba, Carla Rosenberg, Silvia Costa, et al.
Orphanet Journal of Rare Diseases|December 25, 2012
Number of rare germline CNVs and TP53 mutation typesAmanda G Silva, Isabel Maria W Achatz, Ana Cv Krepischi, et al.
Pageof 13