(Q57924143)
Statements
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations (English)
Philippe Debeer
H Peeters
S Driess
L De Smet
K Freese
G Matthijs
D Bornholdt
K Devriendt
K-H Grzeschik
J-P Fryns