Sfoglia per Autore
Unstable translocations: a new case?
file da validare1991-01-01 Mattina, Teresa; Milana, G; D'Agata, A; Conti, L; Sciacca, F.
RFLP analysis in 5 Sicilian families with the fragile X syndrome
file da validare1991-01-01 Romano, V; Mascali, G; Chiavetta, V; Ragusa, Rm; Barletta, C; Romano, C; Mollica, F; Mattina, Teresa; Gross, A; Brown, Wt
COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT
file da validare1992-01-01 Sherman, Sl; Barbi, G; Brondumnielsen, K; Brown, Wt; Carpenter, Nj; Chudley, Ae; Ferraz, Op; Ferreira, P; Gustavson, Kh; Halliday, J; Hockey, A; Howardpeebles, Pn; Jenkins, E; Kennerknecht, I; Kahkonen, M; Ladaique, P; Leisti, J; Maddalena, A; Mazurczak, T; Mattei, Jf; Mattina, Teresa; Mckinley, Mj; Murphy, P; Pellissier, Mc; Purvissmith, S; Robinson, H; Scapagnini, U; Schaap, T; Shapiro, Lr; Smits, Apt; Steinbach, P; Turner, G; Uchida, Ia; Vanoost, Ba; Voelckel, Ma; Weaver, Dd; Webb, T.
Nuovi orizzonti della vecchia genetica.
file da validare1993-01-01 Mollica, F; Mattina, Teresa
Angelman syndrome and vermian cyst
file da validare1994-01-01 Incorpora, G; Cocuzza, M; Mattina, Teresa
The fragile site FrallB, in proto-oncogene CBL-2,is associated with a chromosome deletion syndrome
file da validare1995-01-01 Jones, C.; Penny, L.; Mattina, Teresa; Yu, S.; Baker, E.; Voullaire, L.; Langdon, W. Y.; Sutherland, G. R.; Richards, R. I.; Tunnacliffe, A.
Clinical and Molecular Characterization of Patients with Distal 11q Deletions
file da validare1995-01-01 L. A., Penny; M., Dell'Aquila; M. C., Jones; J., Bergoffen; C., Cunniff; J. P., Fryns; E., Grace; J. M., Graham; B., Kousseff; Mattina, Teresa; J., Syme; L., Voullaire; L., Zelante; J., ZENGER HAIN; O. W., Jones; AND G. A., Evans
Safety and effectiveness of an acellular pertussis vaccine in subjects with Down's syndrome
file da validare1996-01-01 Livolti, S; Mattina, Teresa; Mauro, L; Anfuso, S; Ursino, A; Mollica, F.
Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion
1996-01-01 Gangarossa, S; Schiliro, G; Mattina, Teresa; Scardilli, S; Mollica, F; Cavallari, V.
Antley-Bixler syndrome
file da validare1996-01-01 Mattina, Teresa; Pierluigi, M; Perfumo, C; Mazzone, D; Scardilli, S; Mollica, F.
2. Micromegakarycytes in a patient with partial deletion of the long arm of chromosome 11 del (ll)(q24.2qter)] and chronic thrombocytopenic purpura
file da validare1996-01-01 Gangarossa, S.; Mattina, Teresa; Romano, V.; Milana, G.; Mollica, F.; Schiliro', G.
Double partial trisomy 9q34.1->qter and 21 pter->q22.11:FISH and clinical findings
file da validare1997-01-01 Mattina, Teresa; Pierluigi, M.; Mazzone, D.; Scardilli, S.; Perfumo, C.; Mollica, F.
Multiple minor anomalies and mental retardation in a patient with an interstitial deletion of 4p15 due to 4p/10q translocation.
file da validare1997-01-01 Pierluigi, M; Mattina, Teresa; Perfumo, C; Vinciguerra, E; Bianca, S; Calì, A; Barbagallo, M. A.; Mollica, F; Dagna Bricarelli, F.
Deletion 11q25: clinical cytogenetics, haematological and molecular aspects.
file da validare1997-01-01 Mattina, Teresa; Castiglia, L; Gangarossa, S; Fichera, Marco; Ragusa, C; Vinciguerra, E; Ragusa, A; Mollica, F; Schilirò, G.
Interstitial deletion 2q31q23.2 in a malformed girl. First case report.
file da validare1997-01-01 Barbagallo, ; Mattina, Teresa; Bottaro, Vinciguerra; Bianca, ; Venticinque, Mollica
Triple-X constitution in a child with multiple congenital anomalies
file da validare1998-01-01 Mauceri, L; Baieli, S; Rizzo, Renata; Bianca, S; Mattina, Teresa
La sindrome di Down
file da validare1998-01-01 Mattina, Teresa
Ereditarietà genetica e sclerosi tuberosa
file da validare1998-01-01 Rapisarda, Francesco; Mattina, T.; Infantone, L.; Barbagallo, M. A.; Platania, S.; Milana, G.; Fatuzzo, Pasquale Mario
Complex chromosome rearrangements. Report of three new cases
file da validare1999-01-01 Pierluigi, M.; Mattina, Teresa; Perfumo, C.; Piombo, G.; Zingale, A.; Mandara', G. L.; Fulcheri, E.; DAGNA BRICARELLI, F.
Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998
file da validare1999-01-01 Gaudray, P.; Carle, G. F.; Gerhard, D. S.; Gessler, M.; Mannens, M. M.; Athanasiou, M.; Bliek, J.; Calender, A.; Debelenko, L. V.; Devignes, M. D.; Evans, G. A.; Favier, R.; Forbes, R. S.; Gaudray, G.; Gawin, B.; Gordon, M.; Grimmond, S.; Grossfeld, P.; Harris, J.; Hattori, M.; Hosoda, F.; Hummerich, H.; James, M.; Kalla, J.; Katsanis, N.; Little, P.; Mattina, Teresa; Negrini, M.; Ohki, M.; Osborne Lawrence, S.; Parente, F.; Quincey, D.; Raynaud, S.; Reid, L.; Rethy, L. A.; Schuuring, E.; Sellar, G.; Stilgenbauer, S.; Talbot, C.; Taschner, P.; Thangarajah, T.; Tunnacliffe, A.; Turc Carel, C.; Van Heyningen, V.; Weber, G.; Zabel, B.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Unstable translocations: a new case? | 1-gen-1991 | Mattina, Teresa; Milana, G; D'Agata, A; Conti, L; Sciacca, F. | file da validare |
RFLP analysis in 5 Sicilian families with the fragile X syndrome | 1-gen-1991 | Romano, V; Mascali, G; Chiavetta, V; Ragusa, Rm; Barletta, C; Romano, C; Mollica, F; Mattina, Teresa; Gross, A; Brown, Wt | file da validare |
COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT | 1-gen-1992 | Sherman, Sl; Barbi, G; Brondumnielsen, K; Brown, Wt; Carpenter, Nj; Chudley, Ae; Ferraz, Op; Ferreira, P; Gustavson, Kh; Halliday, J; Hockey, A; Howardpeebles, Pn; Jenkins, E; Kennerknecht, I; Kahkonen, M; Ladaique, P; Leisti, J; Maddalena, A; Mazurczak, T; Mattei, Jf; Mattina, Teresa; Mckinley, Mj; Murphy, P; Pellissier, Mc; Purvissmith, S; Robinson, H; Scapagnini, U; Schaap, T; Shapiro, Lr; Smits, Apt; Steinbach, P; Turner, G; Uchida, Ia; Vanoost, Ba; Voelckel, Ma; Weaver, Dd; Webb, T. | file da validare |
Nuovi orizzonti della vecchia genetica. | 1-gen-1993 | Mollica, F; Mattina, Teresa | file da validare |
Angelman syndrome and vermian cyst | 1-gen-1994 | Incorpora, G; Cocuzza, M; Mattina, Teresa | file da validare |
The fragile site FrallB, in proto-oncogene CBL-2,is associated with a chromosome deletion syndrome | 1-gen-1995 | Jones, C.; Penny, L.; Mattina, Teresa; Yu, S.; Baker, E.; Voullaire, L.; Langdon, W. Y.; Sutherland, G. R.; Richards, R. I.; Tunnacliffe, A. | file da validare |
Clinical and Molecular Characterization of Patients with Distal 11q Deletions | 1-gen-1995 | L. A., Penny; M., Dell'Aquila; M. C., Jones; J., Bergoffen; C., Cunniff; J. P., Fryns; E., Grace; J. M., Graham; B., Kousseff; Mattina, Teresa; J., Syme; L., Voullaire; L., Zelante; J., ZENGER HAIN; O. W., Jones; AND G. A., Evans | file da validare |
Safety and effectiveness of an acellular pertussis vaccine in subjects with Down's syndrome | 1-gen-1996 | Livolti, S; Mattina, Teresa; Mauro, L; Anfuso, S; Ursino, A; Mollica, F. | file da validare |
Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion | 1-gen-1996 | Gangarossa, S; Schiliro, G; Mattina, Teresa; Scardilli, S; Mollica, F; Cavallari, V. | |
Antley-Bixler syndrome | 1-gen-1996 | Mattina, Teresa; Pierluigi, M; Perfumo, C; Mazzone, D; Scardilli, S; Mollica, F. | file da validare |
2. Micromegakarycytes in a patient with partial deletion of the long arm of chromosome 11 del (ll)(q24.2qter)] and chronic thrombocytopenic purpura | 1-gen-1996 | Gangarossa, S.; Mattina, Teresa; Romano, V.; Milana, G.; Mollica, F.; Schiliro', G. | file da validare |
Double partial trisomy 9q34.1->qter and 21 pter->q22.11:FISH and clinical findings | 1-gen-1997 | Mattina, Teresa; Pierluigi, M.; Mazzone, D.; Scardilli, S.; Perfumo, C.; Mollica, F. | file da validare |
Multiple minor anomalies and mental retardation in a patient with an interstitial deletion of 4p15 due to 4p/10q translocation. | 1-gen-1997 | Pierluigi, M; Mattina, Teresa; Perfumo, C; Vinciguerra, E; Bianca, S; Calì, A; Barbagallo, M. A.; Mollica, F; Dagna Bricarelli, F. | file da validare |
Deletion 11q25: clinical cytogenetics, haematological and molecular aspects. | 1-gen-1997 | Mattina, Teresa; Castiglia, L; Gangarossa, S; Fichera, Marco; Ragusa, C; Vinciguerra, E; Ragusa, A; Mollica, F; Schilirò, G. | file da validare |
Interstitial deletion 2q31q23.2 in a malformed girl. First case report. | 1-gen-1997 | Barbagallo, ; Mattina, Teresa; Bottaro, Vinciguerra; Bianca, ; Venticinque, Mollica | file da validare |
Triple-X constitution in a child with multiple congenital anomalies | 1-gen-1998 | Mauceri, L; Baieli, S; Rizzo, Renata; Bianca, S; Mattina, Teresa | file da validare |
La sindrome di Down | 1-gen-1998 | Mattina, Teresa | file da validare |
Ereditarietà genetica e sclerosi tuberosa | 1-gen-1998 | Rapisarda, Francesco; Mattina, T.; Infantone, L.; Barbagallo, M. A.; Platania, S.; Milana, G.; Fatuzzo, Pasquale Mario | file da validare |
Complex chromosome rearrangements. Report of three new cases | 1-gen-1999 | Pierluigi, M.; Mattina, Teresa; Perfumo, C.; Piombo, G.; Zingale, A.; Mandara', G. L.; Fulcheri, E.; DAGNA BRICARELLI, F. | file da validare |
Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998 | 1-gen-1999 | Gaudray, P.; Carle, G. F.; Gerhard, D. S.; Gessler, M.; Mannens, M. M.; Athanasiou, M.; Bliek, J.; Calender, A.; Debelenko, L. V.; Devignes, M. D.; Evans, G. A.; Favier, R.; Forbes, R. S.; Gaudray, G.; Gawin, B.; Gordon, M.; Grimmond, S.; Grossfeld, P.; Harris, J.; Hattori, M.; Hosoda, F.; Hummerich, H.; James, M.; Kalla, J.; Katsanis, N.; Little, P.; Mattina, Teresa; Negrini, M.; Ohki, M.; Osborne Lawrence, S.; Parente, F.; Quincey, D.; Raynaud, S.; Reid, L.; Rethy, L. A.; Schuuring, E.; Sellar, G.; Stilgenbauer, S.; Talbot, C.; Taschner, P.; Thangarajah, T.; Tunnacliffe, A.; Turc Carel, C.; Van Heyningen, V.; Weber, G.; Zabel, B. | file da validare |
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