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Genetics Research|January 13, 2015
Investigation of genetic variants in ubiquitin enzyme genes involved in the modulation of neurodevelopmental processes: a role in schizophrenia susceptibility?Jessica L Andrews, Francesca Fernandez-EnrightGenetics Research|January 13, 2015
Impact of copy number variations burden on coding genome in humans using integrated high resolution arraysAvinash M Veerappa, Kusuma Lingaiah, Sangeetha Vishweswaraiah, et al.Genetics Research|January 13, 2015
Bayesian analysis of additive epistasis arising from new mutations in miceJoaquim Casellas, Daniel Gianola, Juan F MedranoGenetics Research|January 13, 2015
Organization for rare diseases India (ORDI) - addressing the challenges and opportunities for the Indian rare diseases' communityHarsha Karur Rajasimha, Prasannakumar Basayya Shirol, Preveen Ramamoorthy, et al.Genetics Research|January 13, 2015
Bayesian model selection for multiple QTLs mapping combining linkage disequilibrium and linkageDan Jiang, Guoda Ma, Runqing Yang, et al.Genetics Research|January 13, 2015
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patternsYael Laitman, Liat Ries-Levavi, Michal Berkensdadt, et al.Genetics Research|September 15, 2015
The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disordersTony Shen, Ariel Lee, Carol Shen, et al.Genetics Research|June 29, 2016
FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in ChileLorena Santa María, Solange Aliaga, Víctor Faundes, et al.Genetics Research|September 23, 2015
Global patterns of large copy number variations in the human genome reveal complexity in chromosome organizationAvinash M Veerappa, Raviraj V Suresh, Sangeetha Vishweswaraiah, et al.Genetics Research|September 23, 2015
Next generation sequencing for newborn screening: are we there yet?Eitan FriedmanPageof 50