Sfoglia per Autore
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome
1995-01-01 Mari, A; Amati, F; Mingarelli, R; Giannotti, A; Sebastio, G; Colloridi, V; Novelli, G; Dallapiccola, B
Correlation between human papillomavirus type and progressive potential of low grade squamous intra-epithelial dysplastic lesions of the cervix (CIN I)
1995-01-01 Sesti, F; Romanini, C; De Santis, L; Novelli, G; Dallapiccola, B
The link between cytogenetics and mendelism
1995-01-01 Dallapiccola, B; Mingarelli, R; Novelli, G
Molecular Genetics of myotonic dystrophy
1996-01-01 Pizzuti, A; Novelli, G; Dallapiccola, B
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11?
1996-01-01 Digilio, M; Marino, B; Mingarelli, R; Novelli, G; Amati, F; Mari, A; Giannotti, A; Dallapiccola, B
Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency
1996-01-01 Maceratesi, P; Sangiuolo, Fc; Novelli, G; Ninfali, P; Magnani, M; Reichardt, J; Dallapiccola, B
The search for hemizyosity at 22q11 in patients with isolated cleft palate
1996-01-01 Mingarelli, R; Digilio, M; Mari, A; Amati, F; Standoli, L; Giannotti, A; Novelli, G; Dallapiccola, B
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization
1996-01-01 Colosimo, A; Calabrese, G; Gennarelli, M; Ruzzo, A; Sangiuolo, Fc; Magnani, M; Palka, G; Novelli, G; Dallapiccola, B
RFLP discordance in a PKU family due to a deletion in the PAH gene
1996-01-01 Bosco, P; Ceratto, N; Cali, F; Goltsov, Aa; Eisensmith, Rc; Novelli, G; Dalla Piccola, B; Romano, V
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells
1996-02-01 Massari, A; Novelli, G; Colosimo, A; Sangiuolo, Fc; Palka, G; Calabrese, G; Camurri, L; Ghirardini, G; Milani, G; Giorlandino, C; Gazzanelli, G; Malatesta, M; Romanini, C; Dallapiccola, B
Aspetti Genetici della Sordità
1996-04-01 Dallapiccola, B; Mingarelli, R; Gennarelli, M; Novelli, G
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome
1996-04-01 Pizzuti, A; Novelli, G; Mari, A; Ratti, A; Colosimo, A; Amati, F; Penso, D; Sangiuolo, Fc; Calabrese, G; Palka, G; Silani, V; Gennarelli, M; Mingarelli, R; Scarlato, G; Scambler, P; Dallapiccola, B
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
1996-07-01 Pizzuti, A; Amati, F; Calabrese, G; Mari, A; Colosimo, A; Silani, V; Giardino, L; Ratti, A; Penso, D; Calzà, L; Palka, G; Scarlato, G; Novelli, G; Dallapiccola, B
Correlation of SfiI macrorestriction endonuclease fingerprint analysis of Candida parapsilosis isolates with source of isolation
1996-09-01 Pontieri, E; Gregori, L; Gennarelli, M; Ceddia, T; Novelli, G; Dallapiccola, B; De Bernardis, F; Carruba, G
Molecular prenatal diagnosis of neuromuscular disorders
1997-01-01 Dallapiccola, B; Capon, F; Gennarelli, M; Torrente, I; Mingarelli, R; Novelli, G
Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene
1997-01-01 Botta, A; Jurecic, V; Pizzuti, A; Novelli, G; Dallapiccola, B; Baldini, A
The molecular genetics of the DiGeorge syndrome
1997-01-01 Novelli, G; Amati, F; Mari, A; Conti, E; Bengala, M; Telez Sedano, M; Colosimo, A; Sangiuolo, Fc; Scarpino, S; Novelli, A; Sabani, M; Caiola, A; Mingarelli, R; Pizzuti, A; Dallapiccola, B
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvessels
1997-01-13 Lucarelli, M; Gennarelli, M; Cardelli, P; Novelli, G; Scarpa, S; Dallapiccola, B; Strom, R
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
1997-02-01 Pizzuti, A; Novelli, G; Ratti, A; Amati, F; Mari, A; Calabrese, G; Nicolis, S; Silani, V; Marino, B; Scarlato, G; Ottolenghi, S; Dallapiccola, B
Current status of cationic liposome-mediated gene therapy in cystic fibrosis
1998-01-01 Colosimo, A; Sangiuolo, F; Di Sario, S; Serafino, L; Novelli, A; Sabani, M; Castro, M; Lucidi, V; Mossa, G; Dallapiccola, B; Novelli, G
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-1995 | Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome | Mari, A; Amati, F; Mingarelli, R; Giannotti, A; Sebastio, G; Colloridi, V; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1995 | Correlation between human papillomavirus type and progressive potential of low grade squamous intra-epithelial dysplastic lesions of the cervix (CIN I) | Sesti, F; Romanini, C; De Santis, L; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1995 | The link between cytogenetics and mendelism | Dallapiccola, B; Mingarelli, R; Novelli, G | Articolo su rivista | |
1-gen-1996 | Molecular Genetics of myotonic dystrophy | Pizzuti, A; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1996 | Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? | Digilio, M; Marino, B; Mingarelli, R; Novelli, G; Amati, F; Mari, A; Giannotti, A; Dallapiccola, B | Articolo su rivista | |
1-gen-1996 | Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency | Maceratesi, P; Sangiuolo, Fc; Novelli, G; Ninfali, P; Magnani, M; Reichardt, J; Dallapiccola, B | Articolo su rivista | |
1-gen-1996 | The search for hemizyosity at 22q11 in patients with isolated cleft palate | Mingarelli, R; Digilio, M; Mari, A; Amati, F; Standoli, L; Giannotti, A; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1996 | Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization | Colosimo, A; Calabrese, G; Gennarelli, M; Ruzzo, A; Sangiuolo, Fc; Magnani, M; Palka, G; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1996 | RFLP discordance in a PKU family due to a deletion in the PAH gene | Bosco, P; Ceratto, N; Cali, F; Goltsov, Aa; Eisensmith, Rc; Novelli, G; Dalla Piccola, B; Romano, V | Articolo su rivista | |
1-feb-1996 | Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells | Massari, A; Novelli, G; Colosimo, A; Sangiuolo, Fc; Palka, G; Calabrese, G; Camurri, L; Ghirardini, G; Milani, G; Giorlandino, C; Gazzanelli, G; Malatesta, M; Romanini, C; Dallapiccola, B | Articolo su rivista | |
1-apr-1996 | Aspetti Genetici della Sordità | Dallapiccola, B; Mingarelli, R; Gennarelli, M; Novelli, G | Articolo su rivista | |
1-apr-1996 | Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome | Pizzuti, A; Novelli, G; Mari, A; Ratti, A; Colosimo, A; Amati, F; Penso, D; Sangiuolo, Fc; Calabrese, G; Palka, G; Silani, V; Gennarelli, M; Mingarelli, R; Scarlato, G; Scambler, P; Dallapiccola, B | Articolo su rivista | |
1-lug-1996 | cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene | Pizzuti, A; Amati, F; Calabrese, G; Mari, A; Colosimo, A; Silani, V; Giardino, L; Ratti, A; Penso, D; Calzà, L; Palka, G; Scarlato, G; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-set-1996 | Correlation of SfiI macrorestriction endonuclease fingerprint analysis of Candida parapsilosis isolates with source of isolation | Pontieri, E; Gregori, L; Gennarelli, M; Ceddia, T; Novelli, G; Dallapiccola, B; De Bernardis, F; Carruba, G | Articolo su rivista | |
1-gen-1997 | Molecular prenatal diagnosis of neuromuscular disorders | Dallapiccola, B; Capon, F; Gennarelli, M; Torrente, I; Mingarelli, R; Novelli, G | Contributo in libro | |
1-gen-1997 | Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene | Botta, A; Jurecic, V; Pizzuti, A; Novelli, G; Dallapiccola, B; Baldini, A | Articolo su rivista | |
1-gen-1997 | The molecular genetics of the DiGeorge syndrome | Novelli, G; Amati, F; Mari, A; Conti, E; Bengala, M; Telez Sedano, M; Colosimo, A; Sangiuolo, Fc; Scarpino, S; Novelli, A; Sabani, M; Caiola, A; Mingarelli, R; Pizzuti, A; Dallapiccola, B | Articolo su rivista | |
13-gen-1997 | Expression of receptors for native and chemically modified low-density lipoproteins in brain microvessels | Lucarelli, M; Gennarelli, M; Cardelli, P; Novelli, G; Scarpa, S; Dallapiccola, B; Strom, R | Articolo su rivista | |
1-feb-1997 | UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome | Pizzuti, A; Novelli, G; Ratti, A; Amati, F; Mari, A; Calabrese, G; Nicolis, S; Silani, V; Marino, B; Scarlato, G; Ottolenghi, S; Dallapiccola, B | Articolo su rivista | |
1-gen-1998 | Current status of cationic liposome-mediated gene therapy in cystic fibrosis | Colosimo, A; Sangiuolo, F; Di Sario, S; Serafino, L; Novelli, A; Sabani, M; Castro, M; Lucidi, V; Mossa, G; Dallapiccola, B; Novelli, G | Articolo su rivista |
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