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Denise M Kay

Showing results (21-30 of 73) with videos related to

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Birth Defects Research|December 24, 2016
Rare copy number variants in a population-based investigation of hypoplastic right heart syndromeAggeliki Dimopoulos, Robert J Sicko, Denise M Kay, et al.
Annals of Human Genetics|November 7, 2012
Anorectal atresia and variants at predicted regulatory sites in candidate genesTonia C Carter, Denise M Kay, Marilyn L Browne, et al.
American Journal of Medical Genetics. Part A|December 1, 2016
Copy number variants in a population-based investigation of Klippel-Trenaunay syndromeAggeliki Dimopoulos, Robert J Sicko, Denise M Kay, et al.
Journal of the Endocrine Society|August 31, 2022
Whole Exome Sequencing in Patients With Ectopic Posterior PituitaryTatiane S Silva, Fabio R Faucz, Laura C Hernández-Ramírez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 PhenotypeFanny Chasseloup, Nathan Pankratz, John Lane, et al.
Journal of Human Genetics|June 1, 2012
Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiationTonia C Carter, Denise M Kay, Marilyn L Browne, et al.
Annals of Neurology|December 26, 2006
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsDenise M Kay, Dawn Moran, Lina Moses, et al.
Journal of the Endocrine Society|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
Journal of Human Genetics|May 26, 2017
Copy-number variants and candidate gene mutations in isolated split hand/foot malformationTonia C Carter, Robert J Sicko, Denise M Kay, et al.
Human Genetics|January 23, 2008
Exploring gene-environment interactions in Parkinson's diseaseColin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Birth Defects Research|December 24, 2016
Rare copy number variants in a population-based investigation of hypoplastic right heart syndromeAggeliki Dimopoulos, Robert J Sicko, Denise M Kay, et al.
Annals of Human Genetics|November 7, 2012
Anorectal atresia and variants at predicted regulatory sites in candidate genesTonia C Carter, Denise M Kay, Marilyn L Browne, et al.
American Journal of Medical Genetics. Part A|December 1, 2016
Copy number variants in a population-based investigation of Klippel-Trenaunay syndromeAggeliki Dimopoulos, Robert J Sicko, Denise M Kay, et al.
Journal of the Endocrine Society|August 31, 2022
Whole Exome Sequencing in Patients With Ectopic Posterior PituitaryTatiane S Silva, Fabio R Faucz, Laura C Hernández-Ramírez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 PhenotypeFanny Chasseloup, Nathan Pankratz, John Lane, et al.
Journal of Human Genetics|June 1, 2012
Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiationTonia C Carter, Denise M Kay, Marilyn L Browne, et al.
Annals of Neurology|December 26, 2006
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsDenise M Kay, Dawn Moran, Lina Moses, et al.
Journal of the Endocrine Society|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
Journal of Human Genetics|May 26, 2017
Copy-number variants and candidate gene mutations in isolated split hand/foot malformationTonia C Carter, Robert J Sicko, Denise M Kay, et al.
Human Genetics|January 23, 2008
Exploring gene-environment interactions in Parkinson's diseaseColin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Pageof 8