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G Novelli

Showing results (121-130 of 330) with videos related to

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Prenatal Diagnosis|November 1, 1989
Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problemG Novelli, M Frontali, D Baldini, et al.
FEBS Letters|January 13, 1997
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvesselsM Lucarelli, M Gennarelli, P Cardelli, et al.
Muscle & Nerve|March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian familiesF Capon, C Levato, S Semprini, et al.
Gene Therapy|May 29, 2002
Isolation of CF cell lines corrected at DeltaF508-CFTR locus by SFHR-mediated targetingE Bruscia, F Sangiuolo, P Sinibaldi, et al.
American Journal of Medical Genetics|November 1, 1993
Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndromeB Dallapiccola, P Mandich, E Bellone, et al.
Genomics|January 25, 2000
Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndromeA Botta, F Sangiuolo, L Calza, et al.
International Journal of Oral and Maxillofacial Surgery|May 4, 2010
Effectiveness of maxillo-mandibular advancement in obstructive sleep apnea patients with and without skeletal anomaliesP Ronchi, G Novelli, L Colombo, et al.
International Journal of Clinical & Laboratory Research|January 1, 1995
Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassayF Sangiuolo, P Maceratesi, A Mesoraca, et al.
Blood|September 1, 1985
Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stabilityM Magnani, V Stocchi, L Cucchiarini, et al.
Molecular Genetics and Metabolism|April 16, 1998
Human UDP-galactose 4' epimerase (GALE) gene and identification of five missense mutations in patients with epimerase-deficiency galactosemiaP Maceratesi, N Daude, B Dallapiccola, et al.
Pageof 33

Showing results (121-130 of 330) with videos related to

Sort By:
Pageof 33
Prenatal Diagnosis|November 1, 1989
Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problemG Novelli, M Frontali, D Baldini, et al.
FEBS Letters|January 13, 1997
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvesselsM Lucarelli, M Gennarelli, P Cardelli, et al.
Muscle & Nerve|March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian familiesF Capon, C Levato, S Semprini, et al.
Gene Therapy|May 29, 2002
Isolation of CF cell lines corrected at DeltaF508-CFTR locus by SFHR-mediated targetingE Bruscia, F Sangiuolo, P Sinibaldi, et al.
American Journal of Medical Genetics|November 1, 1993
Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndromeB Dallapiccola, P Mandich, E Bellone, et al.
Genomics|January 25, 2000
Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndromeA Botta, F Sangiuolo, L Calza, et al.
International Journal of Oral and Maxillofacial Surgery|May 4, 2010
Effectiveness of maxillo-mandibular advancement in obstructive sleep apnea patients with and without skeletal anomaliesP Ronchi, G Novelli, L Colombo, et al.
International Journal of Clinical & Laboratory Research|January 1, 1995
Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassayF Sangiuolo, P Maceratesi, A Mesoraca, et al.
Blood|September 1, 1985
Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stabilityM Magnani, V Stocchi, L Cucchiarini, et al.
Molecular Genetics and Metabolism|April 16, 1998
Human UDP-galactose 4' epimerase (GALE) gene and identification of five missense mutations in patients with epimerase-deficiency galactosemiaP Maceratesi, N Daude, B Dallapiccola, et al.
Pageof 33