Authors:
MULDERS SM
BICHET DG
RIJSS JPL
KAMSTEEG EJ
ARTHUS MF
LONERGAN M
FUJIWARA M
MORGAN K
LEIJENDEKKER R
VANDERSLUIJS P
VANOS CH
DEEN PMT
Citation: Sm. Mulders et al., AN AQUAPORIN-2 WATER CHANNEL MUTANT WHICH CAUSES AUTOSOMAL-DOMINANT NEPHROGENIC DIABETES-INSIPIDUS IS RETAINED IN THE GOLGI-COMPLEX, The Journal of clinical investigation, 102(1), 1998, pp. 57-66
Authors:
MULDERS SM
BICHET DG
RIJSS JPL
KAMSTEEG EJ
ARTHUS MF
LONERGAN M
FUJIWARA M
MORGAN K
VANOS CH
DEEN PMT
Citation: Sm. Mulders et al., AN AQP2 MUTANT ENCODED IN DOMINANTLY-INHERITED NEPHROGENIC DIABETES-INSIPIDUS IS IMPAIRED IN ITS ROUTING FROM A POST-ENDOPLASMIC RETICULUM COMPARTMENT, Molecular biology of the cell, 8, 1997, pp. 1772-1772
Authors:
MULDERS SM
RIJSS JPL
KAMSTEEG EJ
BICHET DG
VANOS CH
DEEN PMT
Citation: Sm. Mulders et al., AN AQP2 MUTANT ENCODED IN DOMINANTLY-INHERITED NEPHROGENIC DIABETES-INSIPIDUS IS IMPAIRED IN ITS ROUTING FROM A POST-ENDOPLASMIC RETICULUM COMPARTMENT, Journal of the American Society of Nephrology, 8, 1997, pp. 104-104
Authors:
DORUM A
MOLLER P
KAMSTEEG EJ
SCHEFFER H
BURTON M
HEIMDAL KR
MAEHLE LO
HOVIG E
TROPE CG
VANDERHOUT AH
VANDERMEULEN MA
BUYS CHCM
MEERMAN GJT
Citation: A. Dorum et al., A BRCA1 FOUNDER MUTATION, IDENTIFIED WITH HAPLOTYPE ANALYSIS, ALLOWING GENOTYPE PHENOTYPE DETERMINATION AND PREDICTIVE TESTING/, European journal of cancer, 33(14), 1997, pp. 2390-2392
Authors:
HOFSTRA RMW
OSINGA J
TANSINDHUNATA G
WU Y
KAMSTEEG EJ
STULP RP
VANRAVENSWAAIJARTS C
MAJOORKRAKAUER D
ANGRIST M
CHAKRAVARTI A
MEIJERS C
BUYS CHCM
Citation: Rmw. Hofstra et al., A HOMOZYGOUS MUTATION IN THE ENDOTHELIN-3 GENE ASSOCIATED WITH A COMBINED WAARDENBURG TYPE-2 AND HIRSCHSPRUNG PHENOTYPE (SHAH-WAARDENBURG SYNDROME), Nature genetics, 12(4), 1996, pp. 445-447
Authors:
HOFSTRA RMW
STELWAGEN T
STULP RP
DEJONG D
HULSBEEK M
KAMSTEEG EJ
VANDENBERG A
LANDSVATER RM
VERMEY A
MOLENAAR WM
LIPS CJM
BUYS CHCM
Citation: Rmw. Hofstra et al., EXTENSIVE MUTATION SCANNING OF RET IN SPORADIC MEDULLARY-THYROID CARCINOMA AND OF RET AND VHL IN SPORADIC PHEOCHROMOCYTOMA REVEALS INVOLVEMENT OF THESE GENES IN ONLY A MINORITY OF CASES, The Journal of clinical endocrinology and metabolism, 81(8), 1996, pp. 2881-2884
Authors:
HOFSTRA RMW
ANGRIST M
OSINGA J
STULP RP
TAN G
KAMSTEEG EJ
SCHEFFER H
CHAKRAVARTI A
BUYS CHCM
Citation: Rmw. Hofstra et al., MUTATION SCREENING OF THE RET, EDNRB AND ET3 GENES IN HIRSCHSPRUNG PATIENTS, American journal of human genetics, 57(4), 1995, pp. 1110-1110