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Aggeliki Dimopoulos

Showing results (1-10 of 11) with videos related to

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BMJ (Clinical Research Ed.)|February 18, 2016
Authors' reply to Smith and colleaguesJames L Mills, Aggeliki Dimopoulos
BMJ (Clinical Research Ed.)|November 26, 2015
Folic acid fortification for Europe?James L Mills, Aggeliki Dimopoulos
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 16, 2016
What is standing in the way of complete prevention of folate preventable neural tube defects?James L Mills, Aggeliki Dimopoulos, Regan L Bailey
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.
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|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Human Genetics|September 18, 2016
Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathwaysErin M Hagen, Robert J Sicko, Denise M Kay, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
BMJ (Clinical Research Ed.)|February 18, 2016
Authors' reply to Smith and colleaguesJames L Mills, Aggeliki Dimopoulos
BMJ (Clinical Research Ed.)|November 26, 2015
Folic acid fortification for Europe?James L Mills, Aggeliki Dimopoulos
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 16, 2016
What is standing in the way of complete prevention of folate preventable neural tube defects?James L Mills, Aggeliki Dimopoulos, Regan L Bailey
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.
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|December 22, 2017
Corticotropinoma as a Component of Carney ComplexLaura C Hernández-Ramírez, Christina Tatsi, Maya B Lodish, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Human Genetics|September 18, 2016
Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathwaysErin M Hagen, Robert J Sicko, Denise M Kay, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
Pageof 2