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P Gasparini

Showing results (191-200 of 204) with videos related to

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Blood|September 26, 2000
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24S Grootenboer, P O Schischmanoff, I Laurendeau, et al.
American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.
Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.
Scientific Reports|June 7, 2024
Molecular profiling of pediatric and young adult colorectal cancer reveals a distinct genomic landscapes and potential therapeutic avenuesA Busico, P Gasparini, E Rausa, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Annals of Human Genetics|June 21, 2001
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease familiesL Greco, M C Babron, G R Corazza, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Forest Policy and Economics|March 7, 2020
Assessing forest availability for wood supply in EuropeI Alberdi, S Bender, T Riedel, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Pageof 21

Showing results (191-200 of 204) with videos related to

Sort By:
Pageof 21
Blood|September 26, 2000
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24S Grootenboer, P O Schischmanoff, I Laurendeau, et al.
American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.
Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.
Scientific Reports|June 7, 2024
Molecular profiling of pediatric and young adult colorectal cancer reveals a distinct genomic landscapes and potential therapeutic avenuesA Busico, P Gasparini, E Rausa, et al.
Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.
Annals of Human Genetics|June 21, 2001
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease familiesL Greco, M C Babron, G R Corazza, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Forest Policy and Economics|March 7, 2020
Assessing forest availability for wood supply in EuropeI Alberdi, S Bender, T Riedel, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Pageof 21