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Anne C-H Tsai

Showing results (1-10 of 10) with videos related to

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American Journal of Medical Genetics. Part A|July 9, 2011
Revisiting recombinant 8 syndromeLaura Pickler, Rebecca Wilson, Anne C-H Tsai
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 3, 2019
The different facets of "culture" in genetic counseling: A situated analysis of genetic counseling in Hong KongOlga Zayts, Hannah Shipman, Jasmine L-F Fung, et al.
Journal of Autism and Developmental Disorders|February 21, 2019
A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early DevelopmentStuart K Shapira, Lin H Tian, Arthur S Aylsworth, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 23, 2020
Mapping the Relationship between Dysmorphology and Cognitive, Behavioral, and Developmental Outcomes in Children with Autism Spectrum DisorderLin H Tian, Lisa D Wiggins, Laura A Schieve, et al.
Science (New York, N.Y.)|March 26, 2011
Mutations in the RNA granule component TDRD7 cause cataract and glaucomaSalil A Lachke, Fowzan S Alkuraya, Stephen C Kneeland, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterizationCheryl DeScipio, Laura Conlin, Jill Rosenfeld, et al.
Human Mutation|September 18, 2010
Detection of clinically relevant exonic copy-number changes by array CGHPhilip M Boone, Carlos A Bacino, Chad A Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imagingBenedikt Hallgrímsson, J David Aponte, David C Katz, et al.
American Journal of Human Genetics|May 23, 2020
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and OsteochondromasDara Tolchin, Jessica P Yeager, Priya Prasad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 15, 2019
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorderGhayda M Mirzaa, Jessica X Chong, Amélie Piton, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|July 9, 2011
Revisiting recombinant 8 syndromeLaura Pickler, Rebecca Wilson, Anne C-H Tsai
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 3, 2019
The different facets of "culture" in genetic counseling: A situated analysis of genetic counseling in Hong KongOlga Zayts, Hannah Shipman, Jasmine L-F Fung, et al.
Journal of Autism and Developmental Disorders|February 21, 2019
A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early DevelopmentStuart K Shapira, Lin H Tian, Arthur S Aylsworth, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 23, 2020
Mapping the Relationship between Dysmorphology and Cognitive, Behavioral, and Developmental Outcomes in Children with Autism Spectrum DisorderLin H Tian, Lisa D Wiggins, Laura A Schieve, et al.
Science (New York, N.Y.)|March 26, 2011
Mutations in the RNA granule component TDRD7 cause cataract and glaucomaSalil A Lachke, Fowzan S Alkuraya, Stephen C Kneeland, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterizationCheryl DeScipio, Laura Conlin, Jill Rosenfeld, et al.
Human Mutation|September 18, 2010
Detection of clinically relevant exonic copy-number changes by array CGHPhilip M Boone, Carlos A Bacino, Chad A Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imagingBenedikt Hallgrímsson, J David Aponte, David C Katz, et al.
American Journal of Human Genetics|May 23, 2020
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and OsteochondromasDara Tolchin, Jessica P Yeager, Priya Prasad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 15, 2019
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorderGhayda M Mirzaa, Jessica X Chong, Amélie Piton, et al.
Pageof 1