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P Rizzu

Showing results (11-20 of 31) with videos related to

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American Journal of Medical Genetics|February 11, 1997
Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical regionP Rizzu, B R Haddad, I Vallcorba, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mapping segmental imbalances using comparative genomic hybridization and eigenanalysisB Haddad, R Antonacci, P Rizzu, et al.
Genomics|February 15, 1996
A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heartE A Lindsay, P Rizzu, R Antonacci, et al.
Annals of Neurology|October 8, 1999
Phenotypic variation in hereditary frontotemporal dementia with tau mutationsJ C van Swieten, M Stevens, S M Rosso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Annals of Neurology|February 1, 1997
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch familiesP Heutink, M Stevens, P Rizzu, et al.
Genes, Brain, and Behavior|July 6, 2012
Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25T S Rizzi, G Beunders, P Rizzu, et al.
American Journal of Human Genetics|February 11, 1999
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsP Rizzu, J C Van Swieten, M Joosse, et al.
Neuropediatrics|April 19, 2011
Fetal origin of brain damage in 2 infants with a COL4A1 mutation: fetal and neonatal MRIR J Vermeulen, C Peeters-Scholte, J J M Van Vugt, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|February 11, 1997
Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical regionP Rizzu, B R Haddad, I Vallcorba, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mapping segmental imbalances using comparative genomic hybridization and eigenanalysisB Haddad, R Antonacci, P Rizzu, et al.
Genomics|February 15, 1996
A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heartE A Lindsay, P Rizzu, R Antonacci, et al.
Annals of Neurology|October 8, 1999
Phenotypic variation in hereditary frontotemporal dementia with tau mutationsJ C van Swieten, M Stevens, S M Rosso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Annals of Neurology|February 1, 1997
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch familiesP Heutink, M Stevens, P Rizzu, et al.
Genes, Brain, and Behavior|July 6, 2012
Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25T S Rizzi, G Beunders, P Rizzu, et al.
American Journal of Human Genetics|February 11, 1999
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsP Rizzu, J C Van Swieten, M Joosse, et al.
Neuropediatrics|April 19, 2011
Fetal origin of brain damage in 2 infants with a COL4A1 mutation: fetal and neonatal MRIR J Vermeulen, C Peeters-Scholte, J J M Van Vugt, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Pageof 4