|
🐜
|
The spectrum of WRN mutations in Werner syndrome patients
34 auth.
Shurong Huang,
Lin Lee,
N. B. Hanson,
C. Lenaerts,
H. Hoehn,
M. Poot,
C. Rubin,
Da-fu Chen,
Chih-Chao Yang,
Heike Juch,
T. Dorn,
R. Spiegel,
E. Oral,
M. Abid,
C. Battisti,
...
E. Lucci-Cordisco,
G. Neri,
Erin H. Steed,
A. Kidd,
W. Isley,
David Showalter,
J. Vittone,
A. Konstantinow,
J. Ring,
P. Meyer,
S. Wenger,
A. Herbay,
U. Wollina,
M. Schuelke,
Carin R. Huizenga,
Dru F. Leistritz,
G. Martin,
I. Mian,
J. Oshima
|
7 |
2006 |
7
🐜
|
|
🐜
|
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer
25 auth.
A. Viel,
A. Bruselles,
E. Meccia,
M. Fornasarig,
M. Quaia,
V. Canzonieri,
E. Policicchio,
E. Urso,
M. Agostini,
M. Genuardi,
E. Lucci-Cordisco,
T. Venesio,
A. Martayan,
M. Diodoro,
L. Sanchez-Mete,
...
V. Stigliano,
F. Mazzei,
Francesca Grasso,
A. Giuliani,
M. Baiocchi,
R. Maestro,
G. Giannini,
M. Tartaglia,
L. Alexandrov,
M. Bignami
|
7 |
2017 |
7
🐜
|
|
🐜
|
Identification of Muir–Torre syndrome among patients with sebaceous tumors and keratoacanthomas
14 auth.
G. Ponti,
L. Losi,
C. di Gregorio,
L. Roncucci,
M. Pedroni,
A. Scarselli,
P. Benatti,
S. Seidenari,
G. Pellacani,
L. Lembo,
...
G. Rossi,
Massimiliano Marino,
E. Lucci-Cordisco,
M. P. de Leon
|
7 |
2005 |
7
🐜
|
|
🐜
|
Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas.
7 auth.
G. Ponti,
L. Losi,
M. Pedroni,
E. Lucci-Cordisco,
C. di Gregorio,
G. Pellacani,
...
S. Seidenari
|
6 |
2006 |
6
🐜
|
|
🦁
|
Hereditary nonpolyposis colorectal cancer and related conditions
E. Lucci-Cordisco,
I. Zito,
F. Gensini,
M. Genuardi
|
6 |
2003 |
6
🦁
|
|
🐜
|
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer
14 auth.
M. P. Leòn,
P. Benatti,
C. Gregorio,
M. Pedroni,
L. Losi,
M. Genuardi,
A. Viel,
M. Fornasarig,
E. Lucci-Cordisco,
Marcello Anti,
...
G. Ponti,
F. Borghi,
I. Lamberti,
L. Roncucci
|
6 |
2004 |
6
🐜
|
|
🐜
|
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
23 auth.
V. Piccini,
E. Rapizzi,
A. Bacca,
G. Di Trapani,
R. Pulli,
V. Giaché,
B. Zampetti,
E. Lucci-Cordisco,
L. Canu,
E. Corsini,
...
A. Faggiano,
L. Deiana,
D. Carrara,
V. Tantardini,
S. Mariotti,
M. Ambrosio,
M. Zatelli,
G. Parenti,
A. Colao,
C. Pratesi,
G. Bernini,
T. Ercolino,
M. Mannelli
|
6 |
2012 |
6
🐜
|
|
🐜
|
Two PMS2 Mutations in a Turcot Syndrome Family with Small Bowel Cancers
11 auth.
M. Agostini,
M. Tibiletti,
E. Lucci-Cordisco,
A. Chiaravalli,
H. Morreau,
D. Furlan,
...
L. Boccuto,
S. Pucciarelli,
C. Capella,
M. Boiocchi,
A. Viel
|
6 |
2005 |
6
🐜
|
|
🐜
|
High frequency of mosaic CREBBP deletions in Rubinstein-Taybi syndrome patients and mapping of somatic and germ-line breakpoints.
14 auth.
C. Gervasini,
P. Castronovo,
A. Bentivegna,
Federica Mottadelli,
F. Faravelli,
M. Giovannucci-Uzielli,
A. Pessagno,
E. Lucci-Cordisco,
A. Pinto,
L. Salviati,
...
A. Selicorni,
R. Tenconi,
G. Neri,
L. Larizza
|
5 |
2007 |
5
🐜
|
