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Clinical Genetics|December 15, 2015
Application of whole-exome sequencing for detecting copy number variants in CMT1A/HNPPH-Y Jo, M-H Park, H-M Woo, et al.Clinical Genetics|December 17, 2015
Refining the continuum of CFTR-associated disorders in the era of newborn screeningH Levy, M Nugent, K Schneck, et al.Clinical Genetics|November 15, 2017
A critical appraisal of pharmacogenetic inferenceR A J Smit, R Noordam, S le Cessie, et al.Clinical Genetics|December 2, 2017
Genetic association of molecular traits: A help to identify causative variants in complex diseasesC VandiedonckClinical Genetics|November 28, 2017
Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patientsL He, X Pang, H Liu, et al.Clinical Genetics|December 15, 2017
Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansionA T G Chiu, S L C Pei, C C Y Mak, et al.Clinical Genetics|January 1, 1989
Growth, bone maturation and pubertal development in children with the EMG-syndromeW G Sippell, C J Partsch, H R WiedemannClinical Genetics|June 1, 1987
Pallister-Killian syndrome: cytogenetic and molecular studiesP Peltomäki, S Knuutila, A Ritvanen, et al.Clinical Genetics|September 1, 1987
Evidence for a sperm mutation resulting in Duchenne muscular dystrophyA L Børresen, A Heiberg, P Møller, et al.Clinical Genetics|September 8, 2017
Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetranceZ Powis, K D Farwell Hagman, C Mroske, et al.Pageof 718