|
π
|
The Cowden syndrome: a clinical and genetic study in 21 patients
7 auth.
T. Starink,
J. Veen,
F. Arwert,
L. Waal,
G. G. Lange,
J. Gille,
...
A. Eriksson
|
9 |
1986 |
9
π
|
|
π
|
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
16 auth.
M. Levitus,
Q. Waisfisz,
B. Godthelp,
Y. Vries,
S. Hussain,
W. Wiegant,
Elhaam Elghalbzouri-Maghrani,
JΓ»rgen Steltenpool,
M. Rooimans,
G. Pals,
...
F. Arwert,
C. Mathew,
M. Zdzienicka,
K. Hiom,
J. Winter,
H. Joenje
|
8 |
2005 |
8
π
|
|
π
|
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
20 auth.
J. R. Foe,
M. Rooimans,
L. Bosnoyan-Collins,
N. Alon,
M. Wijker,
L. Parker,
J. Lightfoot,
M. Carreau,
D. Callen,
A. Savoia,
...
N. C. Cheng,
C. V. Berkel,
M. Strunk,
J. Gille,
G. Pals,
F. Kruyt,
J. Pronk,
F. Arwert,
M. Buchwald,
H. Joenje
|
8 |
1996 |
8
π
|
|
π
|
The Fanconi anaemia group G gene FANCG is identical with XRCC9
16 auth.
J. Winter,
Q. Waisfisz,
M. Rooimans,
C. V. Berkel,
L. Bosnoyan-Collins,
N. Alon,
M. Carreau,
O. Bender,
I. Demuth,
D. Schindler,
...
J. Pronk,
F. Arwert,
H. Hoehn,
M. Digweed,
M. Buchwald,
H. Joenje
|
8 |
1998 |
8
π
|
|
π
|
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
16 auth.
J. Winter,
M. Rooimans,
L. V. D. Weel,
C. V. Berkel,
N. Alon,
L. Bosnoyan-Collins,
J. D. Groot,
Y. Zhi,
Q. Waisfisz,
J. Pronk,
...
F. Arwert,
C. Mathew,
R. Scheper,
M. Hoatlin,
M. Buchwald,
H. Joenje
|
8 |
2000 |
8
π
|
|
π¬
|
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia
H. Joenje,
F. Arwert,
A. Eriksson,
H. Koning,
A. Oostra
|
8 |
1981 |
8
π¬
|
|
π’
|
Evidence for at least eight Fanconi anemia genes.
11 auth.
H. Joenje,
A. Oostra,
M. Wijker,
F. D. di Summa,
C. V. van Berkel,
M. Rooimans,
...
W. Ebell,
M. V. van Weel,
J. Pronk,
M. Buchwald,
F. Arwert
|
8 |
1997 |
8
π’
|
|
π
|
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
20 auth.
J. Winter,
F. LeΜveilleΜ,
C. V. Berkel,
M. Rooimans,
L. V. D. Weel,
JΓ»rgen Steltenpool,
Ilja Demuth,
N. Morgan,
N. Alon,
L. Bosnoyan-Collins,
...
J. Lightfoot,
P. Leegwater,
Q. Waisfisz,
K. Komatsu,
F. Arwert,
J. Pronk,
C. Mathew,
M. Digweed,
M. Buchwald,
H. Joenje
|
8 |
2000 |
8
π
|
|
π
|
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.
11 auth.
M. Levitus,
M. Rooimans,
JΓ»rgen Steltenpool,
Nicolle F. C. Cool,
A. Oostra,
C. Mathew,
...
M. Hoatlin,
Q. Waisfisz,
F. Arwert,
J. D. de Winter,
H. Joenje
|
7 |
2004 |
7
π
|
|
π
|
Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance
16 auth.
J. R. Foe,
M. Kwee,
M. Rooimans,
A. Oostra,
A. Veerman,
M. V. Weel,
R. Pauli,
N. Shahidi,
I. Dokal,
I. Roberts,
...
Γ. Altay,
E. Gluckman,
R. Gibson,
C. Mathew,
F. Arwert,
H. Joenje
|
7 |
1997 |
7
π
|
|
π
|
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.
10 auth.
J. Winter,
L. V. D. Weel,
J. D. Groot,
S. Stone,
Q. Waisfisz,
F. Arwert,
...
R. Scheper,
FrankA.E. Kruyt,
M. Hoatlin,
H. Joenje
|
7 |
2000 |
7
π
|
