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M Repetto

Showing results (241-250 of 266) with videos related to

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Nature Genetics|February 9, 2024
Advancing diagnosis and research for rare genetic diseases in Indigenous peoplesGareth Baynam, Daria Julkowska, Sarah Bowdin, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 1, 2011
Development of a Tandem-Electrostatic-Quadrupole facility for Accelerator-Based Boron Neutron Capture TherapyA J Kreiner, W Castell, H Di Paolo, et al.
ESMO Open|March 20, 2025
Molecular tumour board in gastrointestinal cancersL Boscolo Bielo, E Crimini, M Repetto, et al.
Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, et al.
Haematologica|May 1, 1983
Bone marrow transplantation for leukemia in GenovaA M Marmont, A Bacigalupo, M T Van Lint, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Nature Medicine|November 10, 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndromeRobert W Davies, Ania M Fiksinski, Elemi J Breetvelt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
New genotype-phenotype correlations and management recommendations for individuals with RERE variantsDavid Curtis, Xiaonan Zhao, Nichole M Owen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
The Lancet. Neurology|December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing studyPhilippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Pageof 27

Showing results (241-250 of 266) with videos related to

Sort By:
Pageof 27
Nature Genetics|February 9, 2024
Advancing diagnosis and research for rare genetic diseases in Indigenous peoplesGareth Baynam, Daria Julkowska, Sarah Bowdin, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 1, 2011
Development of a Tandem-Electrostatic-Quadrupole facility for Accelerator-Based Boron Neutron Capture TherapyA J Kreiner, W Castell, H Di Paolo, et al.
ESMO Open|March 20, 2025
Molecular tumour board in gastrointestinal cancersL Boscolo Bielo, E Crimini, M Repetto, et al.
Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, et al.
Haematologica|May 1, 1983
Bone marrow transplantation for leukemia in GenovaA M Marmont, A Bacigalupo, M T Van Lint, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Nature Medicine|November 10, 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndromeRobert W Davies, Ania M Fiksinski, Elemi J Breetvelt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
New genotype-phenotype correlations and management recommendations for individuals with RERE variantsDavid Curtis, Xiaonan Zhao, Nichole M Owen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
The Lancet. Neurology|December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing studyPhilippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Pageof 27