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Daryl A Scott

Showing results (51-60 of 128) with videos related to

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American Journal of Medical Genetics|April 27, 2002
Performance of cochlear implant recipients with GJB2-related deafnessGlenn E Green, Daryl A Scott, Joshua M McDonald, et al.
Clinical Genetics|March 7, 2026
WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental PhenotypesElyssa Smith, Victor Faundes, Xiaonan Zhao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2CBeata A Nowakowska, Ewa Obersztyn, Krystyna Szymańska, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
Patterns of co-occurring birth defects in children with anotia and microtiaJeremy M Schraw, Renata H Benjamin, Charles J Shumate, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Plos One|January 24, 2014
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, et al.
Pediatric Research|July 1, 2021
Birth defect co-occurrence patterns in the Texas Birth Defects RegistryRenata H Benjamin, Angela E Scheuerle, Daryl A Scott, et al.
Human Molecular Genetics|June 23, 2012
Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1Margaret J Wat, Tyler F Beck, Andrés Hernández-García, et al.
Frontiers in Cell and Developmental Biology|March 22, 2021
<i>OTUD5</i> Variants Associated With X-Linked Intellectual Disability and Congenital MalformationKen Saida, Tokiko Fukuda, Daryl A Scott, et al.
Journal of Pediatric Genetics|November 16, 2018
Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning AlgorithmDanielle A Callaway, Ian M Campbell, Samantha R Stover, et al.
Pageof 13

Showing results (51-60 of 128) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|April 27, 2002
Performance of cochlear implant recipients with GJB2-related deafnessGlenn E Green, Daryl A Scott, Joshua M McDonald, et al.
Clinical Genetics|March 7, 2026
WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental PhenotypesElyssa Smith, Victor Faundes, Xiaonan Zhao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2CBeata A Nowakowska, Ewa Obersztyn, Krystyna Szymańska, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
Patterns of co-occurring birth defects in children with anotia and microtiaJeremy M Schraw, Renata H Benjamin, Charles J Shumate, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Plos One|January 24, 2014
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, et al.
Pediatric Research|July 1, 2021
Birth defect co-occurrence patterns in the Texas Birth Defects RegistryRenata H Benjamin, Angela E Scheuerle, Daryl A Scott, et al.
Human Molecular Genetics|June 23, 2012
Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1Margaret J Wat, Tyler F Beck, Andrés Hernández-García, et al.
Frontiers in Cell and Developmental Biology|March 22, 2021
<i>OTUD5</i> Variants Associated With X-Linked Intellectual Disability and Congenital MalformationKen Saida, Tokiko Fukuda, Daryl A Scott, et al.
Journal of Pediatric Genetics|November 16, 2018
Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning AlgorithmDanielle A Callaway, Ian M Campbell, Samantha R Stover, et al.
Pageof 13