The Inventory of Forest Carbon Stocks in the Province of Trento: some remarks on the sampling design and first comments on its results

Por Gasparini P, Tabacchi G
Publicado em 2008-06-01

International workshop on molecular genetics of haemochromatosis, held at Villa Feltrinelli, Gargnano (Bs), Italy, 25 September 1994.

Por Worwood, M, Gasparini, P, Camaschella, C
Publicado em 1995

TaCAL: a "tariffs" system of tree volume and phytomasses of forest tree species in Calabria (southern Italy)

Por Scrinzi G, Clementel F, Floris A, Gasparini P
Publicado em 2017-02-01

MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies

Por Vuckovic, D., Gasparini, P., Soranzo, N., Iotchkova, V.
Publicado no Bioinformatics (2015)

Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome

Por Athanasakis, E., Biarnés, X., Bonati, M.T., Gasparini, P., Faletra, F.
Publicado em 2012

Alagille Syndrome: A New Missense Mutation Detected by Whole-Exome Sequencing in a Case Previously Found to Be Negative by DHPLC and MLPA

Por Vozzi, D., Licastro, D., Martelossi, S., Athanasakis, E., Gasparini, P., Fabretto, A.
Publicado em 2013

Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family.

Por Gasparini, P, De Fazio, A, Croce, A I, Stanziale, P, Zelante, L
Publicado em 1998

Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR gene.

Por Morral, N., Llevadot, R., Casals, T., Gasparini, P., Macek, M., Dörk, T., Estivill, X.
Publicado em 1994

Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome

Por Athanasakis, E., Fabretto, A., Faletra, F., Mocenigo, M., Morgan, A., Gasparini, P.
Publicado em 2012

Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease.

Por Gasparini, P, Borgo, G, Mastella, G, Bonizzato, A, Dognini, M, Pignatti, P F
Publicado em 1992

Pancreatic function and gene deletion F508 in cystic fibrosis.

Por Borgo, G, Mastella, G, Gasparini, P, Zorzanello, A, Doro, R, Pignatti, P F
Publicado em 1990

Leigh syndrome transmitted by uniparental disomy of chromosome 9

Por TIRANTI, V., LAMANTEA, E., UZIEL, G., ZEVIANI, M., GASPARINI, P., MARZELLA, R., ROCCHI, M., FRIED, M.
Publicado em 1999

Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.

Por Gasparini, P, Miraglia del Giudice, E, Delaunay, J, Totaro, A, Granatiero, M, Melchionda, S, Zelante, L, Iolascon, A
Publicado em 1997

A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23.

Por Amati, P., Gasparini, P., Zlotogora, J., Zelante, L., Chomel, J. C., Kitzis, A., Kaplan, J., Bonneau, D.
Publicado em 1996

Stability and functional effectiveness of phosphorothioate modified duplex DNA and synthetic 'mini-genes'.

Por Ciafrè, S A, Rinaldi, M, Gasparini, P, Seripa, D, Bisceglia, L, Zelante, L, Farace, M G, Fazio, V M
Publicado em 1995

Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

Por Donaudy, F, Zheng, L, Ficarella, R, Ballana, E, Carella, M, Melchionda, S, Estivill, X, Bartles, J R, Gasparini, P
Publicado em 2006

Additive partition of diversity as standard for the selection of protected areas: the natural reserves network of the Siena province (Italy)

Por Marcantonio M, Bacaro G, Filibeck G, Scoppola A, Nonis D, Gasparini P, Rocchini D, Santi E, Landi S, Maccherini S, Chiarucci A
Publicado em 2010-04-01

The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis.

Por Gasparini, P, Novelli, G, Estivill, X, Olivieri, D, Savoia, A, Ruzzo, A, Nunes, V, Borgo, G, Antonelli, M, Williamson, R
Publicado em 1990

A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentation.

Por Nunes, V, Bonizzato, A, Gaona, A, Dognini, M, Chillón, M, Casals, T, Pignatti, P F, Novelli, G, Estivill, X, Gasparini, P
Publicado em 1992

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Por Carella, M, Stewart, G, Ajetunmobi, J F, Perrotta, S, Grootenboer, S, Tchernia, G, Delaunay, J, Totaro, A, Zelante, L, Gasparini, P, Iolascon, A
Publicado em 1998