Search research articles
Contact Us
Filters
Showing results (611-620 of 628) with videos related to
Page
of 63
Sort By:
Community Genetics
|
June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics
A 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 syndrome
M 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 population
A 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 cancer
M 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 cancer
A 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 case
L 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, 1997
J J Holden, M Percy, D Allingham-Hawkins, et al.
International Journal of Immunopathology and Pharmacology
|
January 20, 2011
Vitamins and mast cells
A Anogeianaki, M L Castellani, D Tripodi, et al.
International Journal of Immunopathology and Pharmacology
|
June 13, 2008
Biology of neurotensin: revisited study
G 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 survey
A Sensi, S Cavani, N Villa, et al.
Page
of 63
Search research articles
Search
Showing results (611-620 of 628) with videos related to
Sort By:
Page
of 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 characteristics
A 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 syndrome
M 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 population
A 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 cancer
M 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 cancer
A 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 case
L 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, 1997
J J Holden, M Percy, D Allingham-Hawkins, et al.
International Journal of Immunopathology and Pharmacology
|
January 20, 2011
Vitamins and mast cells
A Anogeianaki, M L Castellani, D Tripodi, et al.
International Journal of Immunopathology and Pharmacology
|
June 13, 2008
Biology of neurotensin: revisited study
G 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 survey
A Sensi, S Cavani, N Villa, et al.
Page
of 63