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A Renieri

Showing results (81-90 of 106) with videos related to

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Journal of Medical Genetics|February 5, 2003
Mild brachydactyly type A1 maps to chromosome 2q35-q36 and is caused by a novel IHH mutation in a three generation familyN Giordano, L Gennari, M Bruttini, et al.
Environmental Research|June 2, 2017
Nonlinear responses to waterborne cadmium exposure in zebrafish. An in vivo studyElisavet A Renieri, Dimitris G Sfakianakis, Athanasios A Alegakis, et al.
European Journal of Medical Genetics|May 22, 2007
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic earsR Caselli, M A Mencarelli, F T Papa, et al.
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 23, 2019
Indicator PCBs in farmed and wild fish in Greece - Risk assessment for the Greek populationElisavet A Renieri, Marina Goumenou, Dmitry A Kardonsky, et al.
European Journal of Medical Genetics|November 8, 2006
2q24-q31 deletion: report of a case and review of the literatureC Pescucci, R Caselli, S Grosso, et al.
Clinical Genetics|January 26, 2008
Three new patients with dup(17)(p11.2p11.2) without autismD Greco, C Romano, S Reitano, et al.
Journal of Human Genetics|May 16, 2007
Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGHR Caselli, C Speciale, C Pescucci, et al.
Clinical Genetics|November 19, 2011
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamicsR De Filippis, L Pancrazi, K Bjørgo, et al.
Clinical Genetics|February 5, 2005
Germline mosaicism in Rett syndrome identified by prenatal diagnosisF Mari, R Caselli, S Russo, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|February 5, 2003
Mild brachydactyly type A1 maps to chromosome 2q35-q36 and is caused by a novel IHH mutation in a three generation familyN Giordano, L Gennari, M Bruttini, et al.
Environmental Research|June 2, 2017
Nonlinear responses to waterborne cadmium exposure in zebrafish. An in vivo studyElisavet A Renieri, Dimitris G Sfakianakis, Athanasios A Alegakis, et al.
European Journal of Medical Genetics|May 22, 2007
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic earsR Caselli, M A Mencarelli, F T Papa, et al.
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 23, 2019
Indicator PCBs in farmed and wild fish in Greece - Risk assessment for the Greek populationElisavet A Renieri, Marina Goumenou, Dmitry A Kardonsky, et al.
European Journal of Medical Genetics|November 8, 2006
2q24-q31 deletion: report of a case and review of the literatureC Pescucci, R Caselli, S Grosso, et al.
Clinical Genetics|January 26, 2008
Three new patients with dup(17)(p11.2p11.2) without autismD Greco, C Romano, S Reitano, et al.
Journal of Human Genetics|May 16, 2007
Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGHR Caselli, C Speciale, C Pescucci, et al.
Clinical Genetics|November 19, 2011
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamicsR De Filippis, L Pancrazi, K Bjørgo, et al.
Clinical Genetics|February 5, 2005
Germline mosaicism in Rett syndrome identified by prenatal diagnosisF Mari, R Caselli, S Russo, et al.
Pageof 11