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Nature Reviews. Genetics|February 4, 2015
A copy number variation map of the human genomeMehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2020
Refining critical regions in 15q24 microdeletion syndrome pertaining to autismYi Liu, Yanqing Zhang, Mehdi Zarrei, et al.
Molecular Phylogenetics and Evolution|November 29, 2011
Speciation and evolution in the Gagea reticulata species complex (Tulipeae; Liliaceae)Mehdi Zarrei, Paul Wilkin, Martin J Ingrouille, et al.
Aob PLANTS|May 1, 2015
DNA barcodes from four loci provide poor resolution of taxonomic groups in the genus CrataegusMehdi Zarrei, Nadia Talent, Maria Kuzmina, et al.
Spine Deformity|October 15, 2024
Genetic overlap between idiopathic scoliosis and schizophrenia in the general populationSteven de Reuver, Worrawat Engchuan, Nickie Safarian, et al.
Plos One|April 22, 2017
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's diseaseNancy J Butcher, Daniele Merico, Mehdi Zarrei, et al.
Journal of Medical Genetics|June 8, 2023
The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samplesMarc Woodbury-Smith, Lia D'Abate, Dimitri J Stavropoulos, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndromeMehdi Zarrei, Daniele Merico, Barbara Kellam, et al.
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