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Domenico Coviello

Showing results (1-10 of 83) with videos related to

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Giornale Italiano Di Cardiologia (2006)|May 17, 2006
[Cardiac cell therapy: the puzzle is waiting to be solved]Marco Canepa, Domenico Coviello, Francesco Chiarella
Toxicology and Applied Pharmacology|July 5, 2005
Medically assisted reproduction and ethical challengesHelena Kääriäinen, Gerry Evers-Kiebooms, Domenico Coviello
European Journal of Human Genetics : EJHG|March 5, 2009
EuroGentest patient information leaflets: a free resource available in over 20 languagesCeline Lewis, Alastair Kent, Heather Skirton, et al.
European Journal of Human Genetics : EJHG|June 15, 2007
An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countriesCeline Lewis, Pritti Mehta, Alastair Kent, et al.
Annals of Pediatric Cardiology|December 19, 2024
Neonatal death of siblings with Uhl's disease and KCNH2 mutation - A rare associationFrancesco Ventura, Rosario Barranco, Francesca Buffelli, et al.
International Journal of Molecular Sciences|March 14, 2017
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant ValidationFrancesca Lantieri, Michela Malacarne, Stefania Gimelli, et al.
European Journal of Human Genetics : EJHG|January 14, 2004
Provision of genetic services in Europe: current practices and issuesBéatrice Godard, Helena Kääriäinen, Ulf Kristoffersson, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literatureSabrina Mariani, Lorenzo Iughetti, Roberto Bertorelli, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 4, 2019
qPCR Applications for the Determination of the Biological AgeMauro Castagnetta, Ulrich Pfeffer, Aldo Chiesa, et al.
Studies in Health Technology and Informatics|November 19, 2021
Interoperability Standards for Data Sharing as a Basis to Fill in a Tailored EHR for Undiagnosed Rare DiseasesNorbert Maggi, Ariam Boaglio, Carmelina Ruggiero, et al.
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Giornale Italiano Di Cardiologia (2006)|May 17, 2006
[Cardiac cell therapy: the puzzle is waiting to be solved]Marco Canepa, Domenico Coviello, Francesco Chiarella
Toxicology and Applied Pharmacology|July 5, 2005
Medically assisted reproduction and ethical challengesHelena Kääriäinen, Gerry Evers-Kiebooms, Domenico Coviello
European Journal of Human Genetics : EJHG|March 5, 2009
EuroGentest patient information leaflets: a free resource available in over 20 languagesCeline Lewis, Alastair Kent, Heather Skirton, et al.
European Journal of Human Genetics : EJHG|June 15, 2007
An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countriesCeline Lewis, Pritti Mehta, Alastair Kent, et al.
Annals of Pediatric Cardiology|December 19, 2024
Neonatal death of siblings with Uhl's disease and KCNH2 mutation - A rare associationFrancesco Ventura, Rosario Barranco, Francesca Buffelli, et al.
International Journal of Molecular Sciences|March 14, 2017
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant ValidationFrancesca Lantieri, Michela Malacarne, Stefania Gimelli, et al.
European Journal of Human Genetics : EJHG|January 14, 2004
Provision of genetic services in Europe: current practices and issuesBéatrice Godard, Helena Kääriäinen, Ulf Kristoffersson, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literatureSabrina Mariani, Lorenzo Iughetti, Roberto Bertorelli, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 4, 2019
qPCR Applications for the Determination of the Biological AgeMauro Castagnetta, Ulrich Pfeffer, Aldo Chiesa, et al.
Studies in Health Technology and Informatics|November 19, 2021
Interoperability Standards for Data Sharing as a Basis to Fill in a Tailored EHR for Undiagnosed Rare DiseasesNorbert Maggi, Ariam Boaglio, Carmelina Ruggiero, et al.
Pageof 9