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Frances Flinter

Showing results (31-40 of 63) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|March 24, 2012
The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993David Vetrie, Igor Vořechovský, Paschalis Sideras, et al.
Pediatric Nephrology (Berlin, Germany)|May 31, 2013
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome, Judy Savige, Elisabet Ars, et al.
Journal of Genetic Counseling|October 11, 2016
Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion GroupsIvan Eisler, Frances Flinter, Jo Grey, et al.
European Journal of Human Genetics : EJHG|October 8, 2015
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery, Ivan Eisler, Matthew Ellison, et al.
Genes|September 28, 2023
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and MiceConstantinos Deltas, Gregory Papagregoriou, Stavroula F Louka, et al.
Pediatric Nephrology (Berlin, Germany)|July 11, 2018
Expert consensus guidelines for the genetic diagnosis of Alport syndromeJudy Savige, Francesca Ariani, Francesca Mari, et al.
Plos One|September 15, 2016
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype CorrelationsJudith Savige, Helen Storey, Hae Il Cheong, et al.
Kidney International|July 3, 2014
The 2014International Workshop on Alport SyndromeJeffrey H Miner, Colin Baigent, Frances Flinter, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
European Journal of Human Genetics : EJHG|September 22, 2016
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disordersKate Wolfe, André Strydom, Deborah Morrogh, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Journal of Immunology (Baltimore, Md. : 1950)|March 24, 2012
The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993David Vetrie, Igor Vořechovský, Paschalis Sideras, et al.
Pediatric Nephrology (Berlin, Germany)|May 31, 2013
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome, Judy Savige, Elisabet Ars, et al.
Journal of Genetic Counseling|October 11, 2016
Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion GroupsIvan Eisler, Frances Flinter, Jo Grey, et al.
European Journal of Human Genetics : EJHG|October 8, 2015
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery, Ivan Eisler, Matthew Ellison, et al.
Genes|September 28, 2023
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and MiceConstantinos Deltas, Gregory Papagregoriou, Stavroula F Louka, et al.
Pediatric Nephrology (Berlin, Germany)|July 11, 2018
Expert consensus guidelines for the genetic diagnosis of Alport syndromeJudy Savige, Francesca Ariani, Francesca Mari, et al.
Plos One|September 15, 2016
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype CorrelationsJudith Savige, Helen Storey, Hae Il Cheong, et al.
Kidney International|July 3, 2014
The 2014International Workshop on Alport SyndromeJeffrey H Miner, Colin Baigent, Frances Flinter, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
European Journal of Human Genetics : EJHG|September 22, 2016
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disordersKate Wolfe, André Strydom, Deborah Morrogh, et al.
Pageof 7