|
π
|
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2
19 auth.
M. F. Amary,
S. Damato,
D. Halai,
M. Eskandarpour,
F. Berisha,
F. Bonar,
S. McCarthy,
V. Fantin,
K. Straley,
S. Lobo,
...
W. Aston,
Claire L. Green,
R. Gale,
R. Tirabosco,
A. Futreal,
P. Campbell,
N. Presneau,
A. Flanagan,
A. Flanagan
|
8 |
2011 |
8
π
|
|
π
|
A common single-nucleotide variant in T is strongly associated with chordoma
19 auth.
N. Pillay,
N. Pillay,
V. Plagnol,
P. Tarpey,
S. Lobo,
N. Presneau,
K. Szuhai,
D. Halai,
F. Berisha,
S. Cannon,
...
S. Mead,
Dalia KasperaviΔiΕ«tΔ,
J. Palmen,
P. Talmud,
L. Kindblom,
M. F. Amary,
R. Tirabosco,
Adrienne M Flanagan,
Adrienne M Flanagan
|
6 |
2012 |
6
π
|
|
π¦
|
Interstitial deletion of 10q: clinical features and literature review.
S. Lobo,
J. Δervenka,
A. London,
M. Pierpont
|
3 |
1992 |
3
π¦
|
