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Showing results (21-30 of 27) with videos related to

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Clinical Genetics|October 16, 2016
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndromeH Dai, V W Zhang, A W El-Hattab, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Double-blind therapeutic trial in Angelman syndrome using betaine and folic acidSarika U Peters, Lynne M Bird, Virginia Kimonis, et al.
Journal of Autism and Developmental Disorders|February 8, 2017
Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 DuplicationsM A Gillentine, L N Berry, R P Goin-Kochel, et al.
Journal of Autism and Developmental Disorders|November 18, 2016
The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 DuplicationsM A Gillentine, L N Berry, R P Goin-Kochel, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Journal of Medical Genetics|March 18, 2009
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disordersS Ben-Shachar, B Lanpher, J R German, et al.
The New England Journal of Medicine|January 8, 2015
TBX6 null variants and a common hypomorphic allele in congenital scoliosisN Wu, X Ming, J Xiao, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Clinical Genetics|October 16, 2016
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndromeH Dai, V W Zhang, A W El-Hattab, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Double-blind therapeutic trial in Angelman syndrome using betaine and folic acidSarika U Peters, Lynne M Bird, Virginia Kimonis, et al.
Journal of Autism and Developmental Disorders|February 8, 2017
Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 DuplicationsM A Gillentine, L N Berry, R P Goin-Kochel, et al.
Journal of Autism and Developmental Disorders|November 18, 2016
The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 DuplicationsM A Gillentine, L N Berry, R P Goin-Kochel, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Journal of Medical Genetics|March 18, 2009
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disordersS Ben-Shachar, B Lanpher, J R German, et al.
The New England Journal of Medicine|January 8, 2015
TBX6 null variants and a common hypomorphic allele in congenital scoliosisN Wu, X Ming, J Xiao, et al.
Pageof 3