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G Novelli

Showing results (161-170 of 330) with videos related to

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Biochemical and Biophysical Research Communications|November 30, 1993
Human elongation factor EF-1 beta: cloning and characterization of the EF1 beta 5a gene and assignment of EF-1 beta isoforms to chromosomes 2,5,15 and XA Pizzuti, M Gennarelli, G Novelli, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patientsM Gennarelli, M Pavoni, P Amicucci, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 9, 2008
Diagnosis of atypical CF: a case-report to reflectF Alghisi, A Angioni, A C Tomaiuolo, et al.
Progress in Clinical and Biological Research|January 1, 1989
DNA marker analysis of adult polycystic kidney disease in Italian families. Italian Cooperative Group on ADPKDL Potenza, P Mandich, G Restagno, et al.
Neurology|November 23, 2005
Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal testsA Botta, A Tacconelli, I Bagni, et al.
Human Mutation|April 11, 2001
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasiaK Pääkkönen, S Cambiaghi, G Novelli, et al.
Human Genetics|October 1, 1995
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndromeA Mari, F Amati, R Mingarelli, et al.
Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.
Clinical Genetics|June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a caseM C Silengo, G F Davi, R Bianco, et al.
The New England Journal of Medicine|October 12, 1989
Laron dwarfism and mutations of the growth hormone-receptor geneS Amselem, P Duquesnoy, O Attree, et al.
Pageof 33

Showing results (161-170 of 330) with videos related to

Sort By:
Pageof 33
Biochemical and Biophysical Research Communications|November 30, 1993
Human elongation factor EF-1 beta: cloning and characterization of the EF1 beta 5a gene and assignment of EF-1 beta isoforms to chromosomes 2,5,15 and XA Pizzuti, M Gennarelli, G Novelli, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patientsM Gennarelli, M Pavoni, P Amicucci, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 9, 2008
Diagnosis of atypical CF: a case-report to reflectF Alghisi, A Angioni, A C Tomaiuolo, et al.
Progress in Clinical and Biological Research|January 1, 1989
DNA marker analysis of adult polycystic kidney disease in Italian families. Italian Cooperative Group on ADPKDL Potenza, P Mandich, G Restagno, et al.
Neurology|November 23, 2005
Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal testsA Botta, A Tacconelli, I Bagni, et al.
Human Mutation|April 11, 2001
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasiaK Pääkkönen, S Cambiaghi, G Novelli, et al.
Human Genetics|October 1, 1995
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndromeA Mari, F Amati, R Mingarelli, et al.
Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.
Clinical Genetics|June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a caseM C Silengo, G F Davi, R Bianco, et al.
The New England Journal of Medicine|October 12, 1989
Laron dwarfism and mutations of the growth hormone-receptor geneS Amselem, P Duquesnoy, O Attree, et al.
Pageof 33