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BMC Medical Genetics|August 20, 2014
Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocksXiaoli Chen, Jun Wang, Elyse Mitchell, et al.Journal of Genetic Counseling|May 22, 2012
The laboratory-clinician team: a professional call to action to improve communication and collaboration for optimal patient care in chromosomal microarray testingKaren E Wain, Erin Riggs, Karen Hanson, et al.American Journal of Human Genetics|June 23, 2015
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationHarrison Brand, Ryan L Collins, Carrie Hanscom, et al.European Journal of Human Genetics : EJHG|May 2, 2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorderSureni V Mullegama, Jill A Rosenfeld, Carmen Orellana, et al.American Journal of Medical Genetics. Part A|October 1, 2015
Recurrent duplications of 17q12 associated with variable phenotypesElyse Mitchell, Andrew Douglas, Susanne Kjaegaard, et al.Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.Pageof 1