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Hywel J Williams

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European Journal of Human Genetics : EJHG|June 11, 2015
STAG3 truncating variant as the cause of primary ovarian insufficiencyPolona Le Quesne Stabej, Hywel J Williams, Chela James, et al.
Biological Psychiatry|January 21, 2004
Support for RGS4 as a susceptibility gene for schizophreniaNigel M Williams, Anna Preece, Gillian Spurlock, et al.
Neurology. Genetics|July 9, 2020
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma geneYing Hong, Annette Keylock, Barbara Jensen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2019
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and ArthrogryposisLouise C Gregory, Pratik Shah, Juliane R F Sanner, et al.
The Journal of Biological Chemistry|February 28, 2004
Identification and analysis of the promoter region of the human hyaluronan synthase 2 geneJamie Monslow, John D Williams, Carol A Guy, et al.
The Journal of Clinical Endocrinology and Metabolism|August 17, 2021
ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian InsufficiencySinéad M McGlacken-Byrne, Polona Le Quesne Stabej, Ignacio Del Valle, et al.
Biological Psychiatry|October 24, 2009
Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approachesMasashi Ikeda, Yasuyuki Tomita, Akihiro Mouri, et al.
Journal of Medical Genetics|July 28, 2018
Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill childrenLamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 1, 2011
Phenotype evaluation and genomewide linkage study of clinical variables in schizophreniaMarian L Hamshere, Peter A Holmans, Geraldine M McCarthy, et al.
Ebiomedicine|March 18, 2019
Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationLouise C Gregory, Carolina B Ferreira, Sara K Young-Baird, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|June 11, 2015
STAG3 truncating variant as the cause of primary ovarian insufficiencyPolona Le Quesne Stabej, Hywel J Williams, Chela James, et al.
Biological Psychiatry|January 21, 2004
Support for RGS4 as a susceptibility gene for schizophreniaNigel M Williams, Anna Preece, Gillian Spurlock, et al.
Neurology. Genetics|July 9, 2020
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma geneYing Hong, Annette Keylock, Barbara Jensen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2019
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and ArthrogryposisLouise C Gregory, Pratik Shah, Juliane R F Sanner, et al.
The Journal of Biological Chemistry|February 28, 2004
Identification and analysis of the promoter region of the human hyaluronan synthase 2 geneJamie Monslow, John D Williams, Carol A Guy, et al.
The Journal of Clinical Endocrinology and Metabolism|August 17, 2021
ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian InsufficiencySinéad M McGlacken-Byrne, Polona Le Quesne Stabej, Ignacio Del Valle, et al.
Biological Psychiatry|October 24, 2009
Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approachesMasashi Ikeda, Yasuyuki Tomita, Akihiro Mouri, et al.
Journal of Medical Genetics|July 28, 2018
Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill childrenLamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 1, 2011
Phenotype evaluation and genomewide linkage study of clinical variables in schizophreniaMarian L Hamshere, Peter A Holmans, Geraldine M McCarthy, et al.
Ebiomedicine|March 18, 2019
Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationLouise C Gregory, Carolina B Ferreira, Sara K Young-Baird, et al.
Pageof 4