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M Miozzo

Showing results (11-20 of 59) with videos related to

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American Journal of Medical Genetics|December 26, 2001
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiencyR Pallotta, L Dalprà, M Miozzo, et al.
Frontiers in Endocrinology|August 29, 2022
Epigenetics of functional hypothalamic amenorrheaL Fontana, E Garzia, G Marfia, et al.
Journal of Clinical and Experimental Neuropsychology|March 1, 1993
Category-specific form-knowledge deficit in a patient with herpes simplex virus encephalitisG Sartori, R Job, M Miozzo, et al.
Clinical Genetics|October 8, 2016
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeL Fontana, B Gentilin, L Fedele, et al.
Journal of Cellular Biochemistry. Supplement|January 1, 1993
Genetic changes in lung cancerU Pastorino, G Sozzi, M Miozzo, et al.
Forensic Science International|January 19, 2010
High throughput analysis of drugs of abuse in hair by combining purposely designed sample extraction compatible with immunometric methods used for drug testing in urineR de la Torre, E Civit, F Svaizer, et al.
Cancer Research|May 15, 1996
Microsatellite alterations in bronchial and sputum specimens of lung cancer patientsM Miozzo, G Sozzi, K Musso, et al.
American Journal of Medical Genetics|January 9, 2001
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotypeF Natacci, L Corrado, M Pierri, et al.
Cancer Genetics and Cytogenetics|January 1, 1990
Chromosome abnormalities and fragile sites in human melanomaG Sozzi, M Miozzo, C Calderone, et al.
Genes, Chromosomes & Cancer|July 1, 1990
t(11;22) in three cases of peripheral neuroepitheliomaM Miozzo, G Sozzi, C Calderone, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|December 26, 2001
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiencyR Pallotta, L Dalprà, M Miozzo, et al.
Frontiers in Endocrinology|August 29, 2022
Epigenetics of functional hypothalamic amenorrheaL Fontana, E Garzia, G Marfia, et al.
Journal of Clinical and Experimental Neuropsychology|March 1, 1993
Category-specific form-knowledge deficit in a patient with herpes simplex virus encephalitisG Sartori, R Job, M Miozzo, et al.
Clinical Genetics|October 8, 2016
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeL Fontana, B Gentilin, L Fedele, et al.
Journal of Cellular Biochemistry. Supplement|January 1, 1993
Genetic changes in lung cancerU Pastorino, G Sozzi, M Miozzo, et al.
Forensic Science International|January 19, 2010
High throughput analysis of drugs of abuse in hair by combining purposely designed sample extraction compatible with immunometric methods used for drug testing in urineR de la Torre, E Civit, F Svaizer, et al.
Cancer Research|May 15, 1996
Microsatellite alterations in bronchial and sputum specimens of lung cancer patientsM Miozzo, G Sozzi, K Musso, et al.
American Journal of Medical Genetics|January 9, 2001
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotypeF Natacci, L Corrado, M Pierri, et al.
Cancer Genetics and Cytogenetics|January 1, 1990
Chromosome abnormalities and fragile sites in human melanomaG Sozzi, M Miozzo, C Calderone, et al.
Genes, Chromosomes & Cancer|July 1, 1990
t(11;22) in three cases of peripheral neuroepitheliomaM Miozzo, G Sozzi, C Calderone, et al.
Pageof 6