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P Gasparini

Showing results (41-50 of 204) with videos related to

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Journal of the American Academy of Dermatology|May 1, 1997
Fixed drug eruptions with feprazone are linked to HLA-B22R Pellicano, M Lomuto, G Ciavarella, et al.
Journal of Neurology|October 1, 1994
The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patientsM Eoli, M Pandolfo, C Milanese, et al.
Annales De Genetique|January 1, 1994
Cytogenetic and molecular analysis of trisomy 9. Case report and reviewL Zelante, A Notarangelo, A I Croce, et al.
Molecular Syndromology|June 27, 2013
Alagille Syndrome: A New Missense Mutation Detected by Whole-Exome Sequencing in a Case Previously Found to Be Negative by DHPLC and MLPAD Vozzi, D Licastro, S Martelossi, et al.
Molecular and Cellular Probes|October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseasesP Gasparini, A Grifa, P Origone, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
Experimental and Clinical Endocrinology|March 1, 1991
Effect of chronic clonidine administration on GH secretion in adult human subjectsA Catania, M Baldini, A Orsatti, et al.
American Journal of Medical Genetics|April 23, 1999
Acrodysplasia, severe ossification abnormalities with short stature, and fibular hypoplasiaA Castriota-Scanderbeg, L Zelante, S Masala, et al.
Tumori|December 31, 1989
Adrenal failure due to bilateral metastases as the sole manifestation of relapsing lung carcinoma. Report of two casesF Guzzini, C Cozzi, F Cortese, et al.
Molecular Syndromology|August 3, 2012
Two Novel COH1 Mutations in an Italian Patient with Cohen SyndromeE Athanasakis, A Fabretto, F Faletra, et al.
Pageof 21

Showing results (41-50 of 204) with videos related to

Sort By:
Pageof 21
Journal of the American Academy of Dermatology|May 1, 1997
Fixed drug eruptions with feprazone are linked to HLA-B22R Pellicano, M Lomuto, G Ciavarella, et al.
Journal of Neurology|October 1, 1994
The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patientsM Eoli, M Pandolfo, C Milanese, et al.
Annales De Genetique|January 1, 1994
Cytogenetic and molecular analysis of trisomy 9. Case report and reviewL Zelante, A Notarangelo, A I Croce, et al.
Molecular Syndromology|June 27, 2013
Alagille Syndrome: A New Missense Mutation Detected by Whole-Exome Sequencing in a Case Previously Found to Be Negative by DHPLC and MLPAD Vozzi, D Licastro, S Martelossi, et al.
Molecular and Cellular Probes|October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseasesP Gasparini, A Grifa, P Origone, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
Experimental and Clinical Endocrinology|March 1, 1991
Effect of chronic clonidine administration on GH secretion in adult human subjectsA Catania, M Baldini, A Orsatti, et al.
American Journal of Medical Genetics|April 23, 1999
Acrodysplasia, severe ossification abnormalities with short stature, and fibular hypoplasiaA Castriota-Scanderbeg, L Zelante, S Masala, et al.
Tumori|December 31, 1989
Adrenal failure due to bilateral metastases as the sole manifestation of relapsing lung carcinoma. Report of two casesF Guzzini, C Cozzi, F Cortese, et al.
Molecular Syndromology|August 3, 2012
Two Novel COH1 Mutations in an Italian Patient with Cohen SyndromeE Athanasakis, A Fabretto, F Faletra, et al.
Pageof 21