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G Neri

Showing results (611-620 of 628) with videos related to

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Community Genetics|June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristicsA Viel, M Genuardi, E Lucci-Cordisco, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Clinical Endocrinology|February 24, 2012
The 312N variant of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR) confers up to 2·7-fold increased risk of polycystic ovary syndrome in a Sardinian populationA Capalbo, F Sagnella, R Apa, et al.
International Journal of Cancer|March 20, 1998
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancerM Genuardi, M Anti, E Capozzi, et al.
Genes, Chromosomes & Cancer|January 1, 1997
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancerA Viel, M Genuardi, E Capozzi, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, et al.
International Journal of Immunopathology and Pharmacology|January 20, 2011
Vitamins and mast cellsA Anogeianaki, M L Castellani, D Tripodi, et al.
International Journal of Immunopathology and Pharmacology|June 13, 2008
Biology of neurotensin: revisited studyG S Katsanos, A Anogianaki, M L Castellani, et al.
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.
Pageof 63

Showing results (611-620 of 628) with videos related to

Sort By:
Pageof 63
Community Genetics|June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristicsA Viel, M Genuardi, E Lucci-Cordisco, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Clinical Endocrinology|February 24, 2012
The 312N variant of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR) confers up to 2·7-fold increased risk of polycystic ovary syndrome in a Sardinian populationA Capalbo, F Sagnella, R Apa, et al.
International Journal of Cancer|March 20, 1998
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancerM Genuardi, M Anti, E Capozzi, et al.
Genes, Chromosomes & Cancer|January 1, 1997
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancerA Viel, M Genuardi, E Capozzi, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, et al.
International Journal of Immunopathology and Pharmacology|January 20, 2011
Vitamins and mast cellsA Anogeianaki, M L Castellani, D Tripodi, et al.
International Journal of Immunopathology and Pharmacology|June 13, 2008
Biology of neurotensin: revisited studyG S Katsanos, A Anogianaki, M L Castellani, et al.
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.
Pageof 63