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American Journal of Human Genetics|December 2, 2019
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal DiagnosisLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Human Mutation|May 28, 2010
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, et al.
Plos Genetics|October 3, 2013
Fusion of large-scale genomic knowledge and frequency data computationally prioritizes variants in epilepsyIan M Campbell, Mitchell Rao, Sean D Arredondo, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2022
Dental data challenge the ubiquitous presence of <i>Homo</i> in the Cradle of HumankindClément Zanolli, Thomas W Davies, Renaud Joannes-Boyau, et al.
Prenatal Diagnosis|November 18, 2008
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 casesIgnatia B Van den Veyver, Ankita Patel, Chad A Shaw, et al.
Pain Reports|February 20, 2020
The Quebec Low Back Pain Study: a protocol for an innovative 2-tier provincial cohortGabrielle M Pagé, Anaïs Lacasse, , et al.
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