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Garavelli

Showing results (421-430 of 609) with videos related to

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Bioinformatics (Oxford, England)|June 27, 2000
PIR: a new resource for bioinformaticsP B McGarvey, H Huang, W C Barker, et al.
Australasian Journal of Ultrasound in Medicine|July 2, 2025
Vertebral Bone Density Abnormalities in Fetal Ultrasound: A Distinctive Clinical Sign of Spondylocarpotarsal Synostosis Syndrome <i>MYH3</i>-RelatedImmacolata Blasi, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.
Plos One|May 6, 2017
Sarcoidosis in an Italian province. Prevalence and environmental risk factorsDeborah Beghè, Luca Dall'Asta, Claudia Garavelli, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineationLivia Garavelli, Anita Wischmeijer, Simonetta Rosato, et al.
Journal of the American Chemical Society|May 18, 2017
Photophysics of Deoxycytidine and 5-Methyldeoxycytidine in Solution: A Comprehensive Picture by Quantum Mechanical Calculations and Femtosecond Fluorescence SpectroscopyL Martínez-Fernández, A J Pepino, J Segarra-Martí, et al.
American Journal of Medical Genetics. Part A|September 28, 2021
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasiaKatarina Cisarova, Livia Garavelli, Stefano Giuseppe Caraffi, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
Genes|September 28, 2023
Diprosopus: A Rare Case of Craniofacial Duplication and a Systematic Review of the LiteratureViola Trevisani, Eleonora Balestri, Manuela Napoli, et al.
Genetic Counseling (Geneva, Switzerland)|March 23, 2007
Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and reviewL Garavelli, S Pedori, R Dal Zotto, et al.
Kidney International|June 22, 2006
Glomerular hyperfiltration predicts the development of microalbuminuria in stage 1 hypertension: the HARVESTP Palatini, P Mormino, F Dorigatti, et al.
Pageof 61

Showing results (421-430 of 609) with videos related to

Sort By:
Pageof 61
Bioinformatics (Oxford, England)|June 27, 2000
PIR: a new resource for bioinformaticsP B McGarvey, H Huang, W C Barker, et al.
Australasian Journal of Ultrasound in Medicine|July 2, 2025
Vertebral Bone Density Abnormalities in Fetal Ultrasound: A Distinctive Clinical Sign of Spondylocarpotarsal Synostosis Syndrome <i>MYH3</i>-RelatedImmacolata Blasi, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.
Plos One|May 6, 2017
Sarcoidosis in an Italian province. Prevalence and environmental risk factorsDeborah Beghè, Luca Dall'Asta, Claudia Garavelli, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineationLivia Garavelli, Anita Wischmeijer, Simonetta Rosato, et al.
Journal of the American Chemical Society|May 18, 2017
Photophysics of Deoxycytidine and 5-Methyldeoxycytidine in Solution: A Comprehensive Picture by Quantum Mechanical Calculations and Femtosecond Fluorescence SpectroscopyL Martínez-Fernández, A J Pepino, J Segarra-Martí, et al.
American Journal of Medical Genetics. Part A|September 28, 2021
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasiaKatarina Cisarova, Livia Garavelli, Stefano Giuseppe Caraffi, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
Genes|September 28, 2023
Diprosopus: A Rare Case of Craniofacial Duplication and a Systematic Review of the LiteratureViola Trevisani, Eleonora Balestri, Manuela Napoli, et al.
Genetic Counseling (Geneva, Switzerland)|March 23, 2007
Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and reviewL Garavelli, S Pedori, R Dal Zotto, et al.
Kidney International|June 22, 2006
Glomerular hyperfiltration predicts the development of microalbuminuria in stage 1 hypertension: the HARVESTP Palatini, P Mormino, F Dorigatti, et al.
Pageof 61