Authors:
DEBOO GM
TIBBEN A
LANSER JBK
JENNEKENSSCHINKEL A
HERMANS J
MAATKIEVIT A
ROOS RAC
Citation: Gm. Deboo et al., EARLY COGNITIVE AND MOTOR SYMPTOMS IN IDENTIFIED CARRIERS OF THE GENEFOR HUNTINGTON-DISEASE, Archives of neurology, 54(11), 1997, pp. 1353-1357
Authors:
HORSTHEMKE B
MAATKIEVIT A
SLEEGERS E
VANDENOUWELAND A
BUITING K
LICH C
MOLLEVANGER P
BEVERSTOCK G
GILLESSENKAESBACH G
SCHWANITZ G
Citation: B. Horsthemke et al., FAMILIAL TRANSLOCATIONS INVOLVING 15Q11-Q13 CAN GIVE RISE TO INTERSTITIAL DELETIONS CAUSING PRADER-WILLI OR ANGELMAN SYNDROME, Journal of Medical Genetics, 33(10), 1996, pp. 848-851
Authors:
SCHRANDERSTUMPEL C
MEINECKE P
WILSON G
GILLESSENKAESBACH G
TINSCHERT S
KONIG R
PHILIP N
RIZZO R
SCHRANDER J
PFEIFFER L
MAATKIEVIT A
VANDERBURGT I
VANESSEN T
LATTA E
HILLIG U
VERLOES A
JOURNEL H
FRYNS JP
Citation: C. Schranderstumpel et al., THE KABUKI (NIIKAWA-KUROKI) SYNDROME - FURTHER DELINEATION OF THE PHENOTYPE IN 29 NON-JAPANESE PATIENTS, European journal of pediatrics, 153(6), 1994, pp. 438-445
Authors:
MAATKIEVIT A
BRUNNER HG
MAASWINKELMOOIJ P
Citation: A. Maatkievit et al., 2 ADDITIONAL CASES OF THE OHDO BLEPHAROPHIMOSIS SYNDROME, American journal of medical genetics, 47(6), 1993, pp. 901-906