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F Caroli

Showing results (61-70 of 79) with videos related to

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American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Molecular and Cellular Probes|July 17, 1998
A method for point mutation analysis that links SSCP and dye primer fluorescent sequencingI Chiarelli, B Porfirio, P L Mattiuz, et al.
Acta Neurochirurgica|January 1, 1990
Mucocele of neurosurgical interest: clinical considerations on five casesA Pompili, R Mastrostefano, F Caroli, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Exclusion of the SCN2B gene as candidate for CMT4BA Bolino, M Seri, F Caroli, et al.
Journal of Neurovirology|June 29, 2000
Dynamics of the reactivity to MBP in multiple sclerosisA Uccelli, G Ristori, D Giunti, et al.
Rheumatology (Oxford, England)|August 22, 2006
Clinical and genetic characterization of Italian patients affected by CINCA syndromeF Caroli, A Pontillo, A D'Osualdo, et al.
European Journal of Endocrinology|February 27, 2008
Uncommon association of germline mutations of RET proto-oncogene and CDKN2A geneL Foppiani, F Forzano, I Ceccherini, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinomaS Bekri, J Adélaïde, S Merscher, et al.
Clinical Genetics|March 22, 2001
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstructionR De Giorgio, M Seri, R Cogliandro, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Molecular and Cellular Probes|July 17, 1998
A method for point mutation analysis that links SSCP and dye primer fluorescent sequencingI Chiarelli, B Porfirio, P L Mattiuz, et al.
Acta Neurochirurgica|January 1, 1990
Mucocele of neurosurgical interest: clinical considerations on five casesA Pompili, R Mastrostefano, F Caroli, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Exclusion of the SCN2B gene as candidate for CMT4BA Bolino, M Seri, F Caroli, et al.
Journal of Neurovirology|June 29, 2000
Dynamics of the reactivity to MBP in multiple sclerosisA Uccelli, G Ristori, D Giunti, et al.
Rheumatology (Oxford, England)|August 22, 2006
Clinical and genetic characterization of Italian patients affected by CINCA syndromeF Caroli, A Pontillo, A D'Osualdo, et al.
European Journal of Endocrinology|February 27, 2008
Uncommon association of germline mutations of RET proto-oncogene and CDKN2A geneL Foppiani, F Forzano, I Ceccherini, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinomaS Bekri, J Adélaïde, S Merscher, et al.
Clinical Genetics|March 22, 2001
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstructionR De Giorgio, M Seri, R Cogliandro, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
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