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M Frontali

Showing results (11-20 of 47) with videos related to

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Gene|July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1E Mantuano, F Trettel, A S Olsen, et al.
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.
American Journal of Medical Genetics|September 1, 1991
Non-random association between DNA markers and Huntington disease locus in the Italian populationA Novelletto, P Mandich, E Bellone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Non-DYT1 dystonia in a large Italian familyA R Bentivoglio, N Del Grosso, A Albanese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 1999
Italian family with cranial cervical dystonia: clinical and genetic studyE Cassetta, N Del Grosso, A R Bentivoglio, et al.
Human Mutation|January 1, 1997
Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriersB Giovannone, G Sabbadini, L Di Maio, et al.
American Journal of Medical Genetics|September 15, 1992
Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndromeF Martino, P D'Eufemia, M S Pergola, et al.
Human Genetics|July 1, 1990
Epidemiological and linkage studies on Huntington's disease in ItalyM Frontali, P Malaspina, C Rossi, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Gene|July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1E Mantuano, F Trettel, A S Olsen, et al.
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.
American Journal of Medical Genetics|September 1, 1991
Non-random association between DNA markers and Huntington disease locus in the Italian populationA Novelletto, P Mandich, E Bellone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Non-DYT1 dystonia in a large Italian familyA R Bentivoglio, N Del Grosso, A Albanese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 1999
Italian family with cranial cervical dystonia: clinical and genetic studyE Cassetta, N Del Grosso, A R Bentivoglio, et al.
Human Mutation|January 1, 1997
Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriersB Giovannone, G Sabbadini, L Di Maio, et al.
American Journal of Medical Genetics|September 15, 1992
Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndromeF Martino, P D'Eufemia, M S Pergola, et al.
Human Genetics|July 1, 1990
Epidemiological and linkage studies on Huntington's disease in ItalyM Frontali, P Malaspina, C Rossi, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
Pageof 5