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Nadia Passon

Showing results (21-30 of 27) with videos related to

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European Journal of Human Genetics : EJHG|November 12, 2020
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotypeCatia Mio, Lorenzo Allegri, Nadia Passon, et al.
Journal of Human Genetics|March 8, 2024
A bird's eye view on the use of whole exome sequencing in rare congenital ophthalmic diseasesJessica Zucco, Federica Baldan, Lorenzo Allegri, et al.
Endocrine Pathology|January 25, 2011
Nucleophosmin delocalization in thyroid tumour cellsAnnalisa Pianta, Cinzia Puppin, Nadia Passon, et al.
Thyroid : Official Journal of the American Thyroid Association|April 19, 2012
Cyclic AMP-response element modulator inhibits the promoter activity of the sodium iodide symporter gene in thyroid cancer cellsNadia Passon, Cinzia Puppin, Elisa Lavarone, et al.
Gene|September 23, 2024
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performanceFederica Baldan, Eliana Demori, Chiara Gnan, et al.
Clinical Endocrinology|September 6, 2012
A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytomaAngela V D'Elia, Franco Grimaldi, Stefano Pizzolitto, et al.
Plos One|August 1, 2012
Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variantsStefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Human Genetics : EJHG|November 12, 2020
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotypeCatia Mio, Lorenzo Allegri, Nadia Passon, et al.
Journal of Human Genetics|March 8, 2024
A bird's eye view on the use of whole exome sequencing in rare congenital ophthalmic diseasesJessica Zucco, Federica Baldan, Lorenzo Allegri, et al.
Endocrine Pathology|January 25, 2011
Nucleophosmin delocalization in thyroid tumour cellsAnnalisa Pianta, Cinzia Puppin, Nadia Passon, et al.
Thyroid : Official Journal of the American Thyroid Association|April 19, 2012
Cyclic AMP-response element modulator inhibits the promoter activity of the sodium iodide symporter gene in thyroid cancer cellsNadia Passon, Cinzia Puppin, Elisa Lavarone, et al.
Gene|September 23, 2024
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performanceFederica Baldan, Eliana Demori, Chiara Gnan, et al.
Clinical Endocrinology|September 6, 2012
A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytomaAngela V D'Elia, Franco Grimaldi, Stefano Pizzolitto, et al.
Plos One|August 1, 2012
Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variantsStefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, et al.
Pageof 3