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M Repetto

Showing results (221-230 of 266) with videos related to

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Journal of Magnetic Resonance (San Diego, Calif. : 1997)|March 2, 2016
HP-Xe to go: Storage and transportation of hyperpolarized (129)XenonM Repetto, S Zimmer, F Allmendinger, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
Probable identity-by-descent for a mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia (Dymeclin) gene among patients from Guam, Chile, Argentina, and SpainRobert Pogue, Nadia Ehtesham, Gabriela M Repetto, et al.
American Journal of Medical Genetics. Part A|June 12, 2023
PUF60-related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variantsH Grimes, M Ansari, T Ashraf, et al.
Brain : a Journal of Neurology|April 4, 2017
Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's diseaseNancy J Butcher, Connie Marras, Margarita Pondal, et al.
Psychoneuroendocrinology|April 12, 2021
Evaluation of stress, burnout and hair cortisol levels in health workers at a University Hospital during COVID-19 pandemicCarolina Ibar, Federico Fortuna, Diego Gonzalez, et al.
Journal of Human Genetics|August 17, 2004
Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfateShunji Tomatsu, Tatiana Dieter, Ida V Schwartz, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 18, 2021
ESMO recommendations on the standard methods to detect RET fusions and mutations in daily practice and clinical researchC Belli, F Penault-Llorca, M Ladanyi, et al.
Revista Chilena De Infectologia : Organo Oficial De La Sociedad Chilena De Infectologia|December 21, 2019
[Sociodemographic risk factors of hantavirus cardiopulmonary syndrome]Cecilia Vial C, Francisca Valdivieso R, Analía Cuiza V, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
International Journal of Dermatology|September 4, 2021
Prevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitisGeovanna V Cárdenas, Carolina Iturriaga, Caroll D Hernández, et al.
Pageof 27

Showing results (221-230 of 266) with videos related to

Sort By:
Pageof 27
Journal of Magnetic Resonance (San Diego, Calif. : 1997)|March 2, 2016
HP-Xe to go: Storage and transportation of hyperpolarized (129)XenonM Repetto, S Zimmer, F Allmendinger, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
Probable identity-by-descent for a mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia (Dymeclin) gene among patients from Guam, Chile, Argentina, and SpainRobert Pogue, Nadia Ehtesham, Gabriela M Repetto, et al.
American Journal of Medical Genetics. Part A|June 12, 2023
PUF60-related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variantsH Grimes, M Ansari, T Ashraf, et al.
Brain : a Journal of Neurology|April 4, 2017
Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's diseaseNancy J Butcher, Connie Marras, Margarita Pondal, et al.
Psychoneuroendocrinology|April 12, 2021
Evaluation of stress, burnout and hair cortisol levels in health workers at a University Hospital during COVID-19 pandemicCarolina Ibar, Federico Fortuna, Diego Gonzalez, et al.
Journal of Human Genetics|August 17, 2004
Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfateShunji Tomatsu, Tatiana Dieter, Ida V Schwartz, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 18, 2021
ESMO recommendations on the standard methods to detect RET fusions and mutations in daily practice and clinical researchC Belli, F Penault-Llorca, M Ladanyi, et al.
Revista Chilena De Infectologia : Organo Oficial De La Sociedad Chilena De Infectologia|December 21, 2019
[Sociodemographic risk factors of hantavirus cardiopulmonary syndrome]Cecilia Vial C, Francisca Valdivieso R, Analía Cuiza V, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
International Journal of Dermatology|September 4, 2021
Prevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitisGeovanna V Cárdenas, Carolina Iturriaga, Caroll D Hernández, et al.
Pageof 27