P Mandich|E Bellone|A Massari|F Ajmar - JoVE Visualize

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Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1991

Polymerase chain reaction (PCR) amplification of hypervariable genomic sequencesP Mandich, E Bellone, A Massari, et al.

American Journal of Medical Genetics|May 1, 1991

Genetic analysis of Huntington disease in ItalyF Ajmar, P Mandich, E Bellone, et al.

Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1991

Adult polycystic kidney disease: prenatal diagnosis with DNA polymorphic markersE Bellone, P Mandich, P Costa, et al.

Bollettino Della Societa Italiana Di Biologia Sperimentale|April 1, 1992

Charcot-Marie-Tooth disease: evidence of a duplication at D17S122 locusP Mandich, E Bellone, A Uccelli, et al.

European Neurology|January 1, 1996

Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's diseaseP Mandich, E Di Maria, E Bellone, 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.

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.

Genomics|July 1, 1994

Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12P Mandich, A M Schito, E Bellone, et al.

Neuroscience Letters|July 26, 1996

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patientsE Bellone, A Schenone, G Mancardi, et al.

Human Mutation|September 30, 1999

A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 diseaseE Bellone, E Di Maria, S Soriani, et al.

Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:

Pageof 15

Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1991

Polymerase chain reaction (PCR) amplification of hypervariable genomic sequencesP Mandich, E Bellone, A Massari, et al.

American Journal of Medical Genetics|May 1, 1991

Genetic analysis of Huntington disease in ItalyF Ajmar, P Mandich, E Bellone, et al.

Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1991

Adult polycystic kidney disease: prenatal diagnosis with DNA polymorphic markersE Bellone, P Mandich, P Costa, et al.

Bollettino Della Societa Italiana Di Biologia Sperimentale|April 1, 1992

Charcot-Marie-Tooth disease: evidence of a duplication at D17S122 locusP Mandich, E Bellone, A Uccelli, et al.

European Neurology|January 1, 1996

Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's diseaseP Mandich, E Di Maria, E Bellone, 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.

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.

Genomics|July 1, 1994

Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12P Mandich, A M Schito, E Bellone, et al.

Neuroscience Letters|July 26, 1996

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patientsE Bellone, A Schenone, G Mancardi, et al.

Human Mutation|September 30, 1999

A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 diseaseE Bellone, E Di Maria, S Soriani, et al.

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