(Q34957544)
Statements
1 reference
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype (English)
1 reference
T Kleefstra
1 reference
W A van Zelst-Stams
1 reference
W M Nillesen
1 reference
V Cormier-Daire
1 reference
G Houge
1 reference
N Foulds
1 reference
M van Dooren
1 reference
M H Willemsen
1 reference
R Pfundt
1 reference
A Turner
1 reference
M Wilson
1 reference
A Rauch
1 reference
M Zenker
1 reference
M P Adam
1 reference
C Davies
1 reference
A González-Meneses López
1 reference
R Casalone
1 reference
A Weber
1 reference
L A Brueton
1 reference
A Delicado Navarro
1 reference
M Palomares Bralo
1 reference
S P A Stegmann
1 reference
H G Yntema
1 reference
H van Bokhoven
1 reference
H G Brunner
1 reference
4 March 2009
1 reference
1 reference
46
1 reference
9
1 reference
598-606
1 reference
Identifiers
1 reference
1 reference