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Catherine Deveault

Showing results (1-10 of 8) with videos related to

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Ophthalmic Genetics|April 6, 2011
BBS mutational analysis: a strategic approachGail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics|May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactylyGail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Human Mutation|June 21, 2007
Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutationsJinhua Qian, Catherine Deveault, Rashmi Bagga, et al.
Journal of Pediatric and Adolescent Gynecology|May 18, 2016
Anti-Müllerian Hormone in Female Adolescent Cancer Patients Before, During, and After Completion of Therapy: A Pilot Feasibility StudyAbha A Gupta, Amy Lee Chong, Catherine Deveault, et al.
Human Molecular Genetics|December 11, 2008
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formationCatherine Deveault, Jian Hua Qian, Wafaa Chebaro, et al.
Pediatric Blood & Cancer|December 23, 2017
Pediatric oncology clinical trial participation where the geography is vast: Development of a clinical research system for tertiary and satellite centers in Ontario, CanadaSarah Alexander, Mark Greenberg, David Malkin, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Human Mutation|February 24, 2011
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definitionCatherine Deveault, Gail Billingsley, Jacque L Duncan, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Ophthalmic Genetics|April 6, 2011
BBS mutational analysis: a strategic approachGail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics|May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactylyGail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Human Mutation|June 21, 2007
Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutationsJinhua Qian, Catherine Deveault, Rashmi Bagga, et al.
Journal of Pediatric and Adolescent Gynecology|May 18, 2016
Anti-Müllerian Hormone in Female Adolescent Cancer Patients Before, During, and After Completion of Therapy: A Pilot Feasibility StudyAbha A Gupta, Amy Lee Chong, Catherine Deveault, et al.
Human Molecular Genetics|December 11, 2008
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formationCatherine Deveault, Jian Hua Qian, Wafaa Chebaro, et al.
Pediatric Blood & Cancer|December 23, 2017
Pediatric oncology clinical trial participation where the geography is vast: Development of a clinical research system for tertiary and satellite centers in Ontario, CanadaSarah Alexander, Mark Greenberg, David Malkin, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Human Mutation|February 24, 2011
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definitionCatherine Deveault, Gail Billingsley, Jacque L Duncan, et al.
Pageof 1