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American Journal of Medical Genetics. Part A|October 31, 2014
4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence of KIT haploinsufficiencyParisa Hemati, Christèle du Souich, Cornelius F Boerkoel
Journal of Genetic Counseling|April 10, 2019
Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unitEmma E Smith, Christèle du Souich, Nick Dragojlovic, et al.
American Journal of Medical Genetics. Part A|March 3, 2009
A novel syndrome with psychiatric features and review of malformation syndromes with psychiatric disordersChristèle du Souich, Jehannine C Austin, Robin Friedlander, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Coffin-Siris syndrome: phenotypic evolution of a novel SMARCA4 mutationMichael Tzeng, Christèle du Souich, Helen Wing-Hong Cheung, et al.
Journal of Molecular Histology|November 25, 2011
Expression profile of NSDHL in human peripheral tissuesMarie Morimoto, Christèle du Souich, Joanne Trinh, et al.
Journal of Genetic Counseling|June 24, 2021
After genomic testing results: Parents' long-term viewsNicole Si Yan Liang, Shelin Adam, Alison M Elliott, et al.
American Journal of Medical Genetics. Part A|September 9, 2017
FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?Angela Myers, Christèle du Souich, Connie L Yang, et al.
Molecular Genetics & Genomic Medicine|June 1, 2018
The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British ColumbiaAlison M Elliott, Christèle du Souich, Shelin Adam, et al.
Journal of Telemedicine and Telecare|January 20, 2021
Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES StudyAlison M Elliott, Nick Dragojlovic, Teresa Campbell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking studyNick Dragojlovic, Alison M Elliott, Shelin Adam, et al.
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