ACNP - Italian Periodicals Catalogue

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Results: 1-12 |

Results: 12

A single strand conformation polymorphism-based carrier test for spinal muscular atrophy

Authors: Semprini, S Tacconelli, A Capon, F Brancati, F Dallapiccola, B Novelli, G

Citation: S. Semprini et al., A single strand conformation polymorphism-based carrier test for spinal muscular atrophy, GENET TEST, 5(1), 2001, pp. 33-37

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26

Authors: Mangino, M Flex, E Capon, F Sangiuolo, F Carraro, E Gualandi, F Mazzoli, M Martini, A Novelli, G Dallapiccola, B

Citation: M. Mangino et al., Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26, EUR J HUM G, 9(9), 2001, pp. 667-671

Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21

Authors: Capon, F Semprini, S Chimenti, S Fabrizi, G Zambruno, G Murgia, S Carcassi, C Fazio, M Mingarelli, R Dallapiccola, B Novelli, G

Citation: F. Capon et al., Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21, J INVES DER, 116(5), 2001, pp. 728-730

Advances in the search for psoriasis susceptibility genes

Authors: Capon, F Dallapiccola, B Novelli, G

Citation: F. Capon et al., Advances in the search for psoriasis susceptibility genes, MOL GEN MET, 71(1-2), 2000, pp. 250-255

Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3

Authors: Sangiuolo, F Bruscia, E Capon, F Servidei, S Dallapiccola, B Novelli, G

Citation: F. Sangiuolo et al., Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3, EUR J HUM G, 8(10), 2000, pp. 809-812

Mapping a dominant form of multinodular goiter to chromosome Xp22

Authors: Capon, F Tacconelli, A Giardina, E Sciacchitano, S Bruno, R Tassi, V Trischitta, V Filetti, S Dallapiccola, B Noveili, G

Citation: F. Capon et al., Mapping a dominant form of multinodular goiter to chromosome Xp22, AM J HU GEN, 67(4), 2000, pp. 1004-1007

Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility

Authors: Semprini, S Capon, F Bovolenta, S Bruscia, E Pizzuti, L Fabrizi, G Schietroma, C Zambruno, G Dallapiccola, B Novelli, G

Citation: S. Semprini et al., Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility, HUM GENET, 104(2), 1999, pp. 130-134

Expression and activation of pro-gelatinase A by human melanoma cell lineswith different tumorigenic potential

Authors: Capon, F Emonard, H Hornebeck, W Maquart, FX Bernard, P

Citation: F. Capon et al., Expression and activation of pro-gelatinase A by human melanoma cell lineswith different tumorigenic potential, CLIN EXP M, 17(6), 1999, pp. 463-469

A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13

Authors: Servidei, S Capon, F Spinazzola, A Mirabella, M Semprini, S de Rosa, G Gennarelli, M Sangiuolo, F Ricci, E Mohrenweiser, HW Dallapiccola, B Tonali, P Novelli, G

Citation: S. Servidei et al., A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13, NEUROLOGY, 53(4), 1999, pp. 830-837

Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1

Authors: Capon, F Novelli, G Semprini, S Clementi, M Nudo, M Vultaggio, P Mazzanti, C Gobello, T Botta, A Fabrizi, G Dallapiccola, B

Citation: F. Capon et al., Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1, J INVES DER, 112(1), 1999, pp. 32-35

Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21

Authors: Capon, F Semprini, S Dallapiccola, B Novelli, G

Citation: F. Capon et al., Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21, AM J HU GEN, 65(6), 1999, pp. 1798-1800

Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22

Authors: Mangino, M Sanchez, O Torrente, I De Luca, A Capon, F Novelli, G Dallapiccola, B

Citation: M. Mangino et al., Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22, AM J HU GEN, 65(2), 1999, pp. 441-447

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