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DEMEIRLEIR L
LISSENS W
BENELLI C
MARSAC C
DEKLERK J
SCHOLTE J
VANDIGGELEN O
KLEIJER W
SENECA S
LIEBAERS I
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Authors:
VANROYENKERKHOF A
POLLTHE BT
KLEIJER W
VANDIGGELEN OP
AERTS JMFG
HOPWOOD JJ
BEEMER FA
Citation: A. Vanroyenkerkhof et al., COEXISTENCE OF GAUCHER-DISEASE TYPE-1 AND JOUBERT-SYNDROME, Journal of Medical Genetics, 35(11), 1998, pp. 965-966
Authors:
TAYEBI N
CUSHNER SR
KLEIJER W
LAU EK
DAMSCHRODERWILLIAMS PJ
STUBBLEFIELD BK
DENHOLLANDER J
SIDRANSKY E
Citation: N. Tayebi et al., PRENATAL LETHALITY OF A HOMOZYGOUS NULL MUTATION IN THE HUMAN GLUCOCEREBROSIDASE GENE, American journal of medical genetics, 73(1), 1997, pp. 41-47
Authors:
VAZKEN M
DERKALOUSTIAN MD
KLEIJER W
VEKEMANS M
MAZER B
ELLIOTT AM
BOOTH A
ABISH S
EYDOUX P
Citation: M. Vazken et al., A NEW VARIANT OF THE NIJMEGEN BREAKAGE SYNDROME WITH MULTIPLE NONSPECIFIC CHROMOSOMAL-ANOMALIES AND A PARTICULAR PHENOTYPE, American journal of human genetics, 57(4), 1995, pp. 624-624