P. Vignetti
发表
A novel double nucleotide substitution in the HMG box of the SRY gene associated with Swyer syndrome
L. Bruni,
R. Verna,
E. D’Ambrosio,
1997,
Human Genetics.
G. Raguso,
L. Tarani,
F. Colloridi,
1994,
Annales de genetique.
P. Curatolo,
R. Cusmai,
P. Vignetti,
1986,
European Journal of Pediatrics.
G. Nucci,
R. Cerbo,
L. Tarani,
1995,
European Journal of Pediatrics.
M. Antonelli,
P. Vignetti,
M. Dahir,
1987,
Transactions of the Royal Society of Tropical Medicine and Hygiene.
B. Dallapiccola,
L. Chessa,
P. Vignetti,
2004,
Human Genetics.
B. Dallapiccola,
L. Chessa,
L. Bruni,
1977,
Clinical genetics.
P. Vignetti,
E. Ferrante,
L. Capotorti,
1966,
Minerva pediatrica.
C. Cappelli,
F. Cozzi,
L. Tarani,
1992,
European Journal of Pediatrics.
A. Pasquino,
B. Dallapiccola,
L. Chessa,
1980,
Journal of medical genetics.
L. Chessa,
L. Bruni,
M. Antonelli,
1983,
Helvetica paediatrica acta.
L. Bruni,
G. Finocchi,
B. Boscherini,
1977,
Minerva pediatrica.
L. Tarani,
L. Bruni,
A. Rizzuti,
1996,
International journal of sports medicine.
P. Vignetti,
E. Ferrante,
L. Capotorti,
1964,
The Lancet.
D. Roos,
L. Bruni,
R. Corbo,
1978,
Pediatric Research.
C. Dominici,
M. Castello,
A. Clerico,
1987,
Tumori.