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M Seri

Showing results (21-30 of 73) with videos related to

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European Journal of Immunology|February 17, 2001
Characterization of the response to myelin basic protein in a non human primate model for multiple sclerosisA Uccelli, D Giunti, G Mancardi, et al.
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.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, 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.
International Journal of Molecular Medicine|October 10, 2002
MICA gene polymorphisms in an Italian paediatric series of juvenile Behçet diseaseP Picco, B Porfirio, M Gattorno, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Oncogene|June 15, 1995
RET mutations in exons 13 and 14 of FMTC patientsA Bolino, I Schuffenecker, Y Luo, et al.
Epilepsy Research|April 12, 2014
LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF)P Magini, F Bisulli, S Baldassari, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
European Journal of Immunology|February 17, 2001
Characterization of the response to myelin basic protein in a non human primate model for multiple sclerosisA Uccelli, D Giunti, G Mancardi, et al.
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.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, 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.
International Journal of Molecular Medicine|October 10, 2002
MICA gene polymorphisms in an Italian paediatric series of juvenile Behçet diseaseP Picco, B Porfirio, M Gattorno, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Oncogene|June 15, 1995
RET mutations in exons 13 and 14 of FMTC patientsA Bolino, I Schuffenecker, Y Luo, et al.
Epilepsy Research|April 12, 2014
LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF)P Magini, F Bisulli, S Baldassari, et al.
Pageof 8