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Authors: KISHORE A WSZOLEK ZK SNOW BJ DELAFUENTEFERNANDEZ R ARWERT F WIJKER M SCHULZER M CALNE DB VINGERHOETS FJG
Citation: A. Kishore et al., PRESYNAPTIC NIGROSTRIATAL FUNCTION IN GENETICALLY TESTED ASYMPTOMATICRELATIVES FROM THE PALLIDO-PONTO-NIGRAL DEGENERATION FAMILY, Neurology, 47(6), 1996, pp. 1588-1590

Authors: ABRAHAMS PJ HOUWELING A CORNELISSENSTEIJGER PDM ARWERT F MENKO FH
Citation: Pj. Abrahams et al., INHERITANCE OF ABNORMAL EXPRESSION OF SOS-LIKE RESPONSE IN XERODERMA-PIGMENTOSUM AND HEREDITARY CANCER-PRONE SYNDROMES, Cancer research, 56(11), 1996, pp. 2621-2625

Authors: PRONK JC GIBSON RA SAVOIA A WIJKER M MORGAN NV MELCHIONDA S FORD D TEMTAMY S ORTEGA JJ JANSEN S HAVENGA C COHN RJ DERAVEL TJ ROBERTS I WESTERVELD A EASTON DF JOENJE H MATHEW CG ARWERT F
Citation: Jc. Pronk et al., LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3, Nature genetics, 11(3), 1995, pp. 338-340

Authors: WILHELMSEN KC LYNCH T ARWERT F WSZOLEK Z
Citation: Kc. Wilhelmsen et al., 2 LARGE PARKINSONIAN KINDREDS LINKED TO WLD LOCUS ON CHROMOSOME-17Q-21-22, Annals of neurology, 38(2), 1995, pp. 301-301

Authors: STEENBERGEN RDM HERMSEN MAJA WALBOOMERS JMM JOENJE H ARWERT F MEIJER CJLM SNIJDERS PJF
Citation: Rdm. Steenbergen et al., INTEGRATED HUMAN PAPILLOMAVIRUS TYPE-16 AND LOSS OF HETEROZYGOSITY AT11Q22 AND 18Q21 IN AN ORAL-CARCINOMA AND ITS DERIVATIVE CELL-LINE, Cancer research, 55(22), 1995, pp. 5465-5471

Authors: JOENJE H TENFOE JRL OOSTRA AB VANBERKEL CGN ROOIMANS MA SCHROEDERKURTH T WEGNER RD GILLE JJP BUCHWALD M ARWERT F
Citation: H. Joenje et al., CLASSIFICATION OF FANCONI-ANEMIA PATIENTS BY COMPLEMENTATION ANALYSIS- EVIDENCE FOR A 5TH GENETIC SUBTYPE, Blood, 86(6), 1995, pp. 2156-2160

Authors: WIJKER M LIGTENBERG MJL SCHOUTE F DEFESCHE JC PALS G BOLHUIS PA ROPERS HH HULSEBOS TJM MENKO FH VANOOST BA LUNGAROTTI MS ARWERT F
Citation: M. Wijker et al., THE GENE FOR HEREDITARY BULLOUS DYSTROPHY, X-LINKED MACULAR TYPE, MAPS TO THE XQ27.3-QTER REGION, American journal of human genetics, 56(5), 1995, pp. 1096-1100

Authors: SCHEPENS M NIEUWINT A VANDEVELDEVISSER S MERK G VANKESSEL AG OVERHAUSER J DONNAI D ARWERT F HAMEL B MENKO F MARIMAN E
Citation: M. Schepens et al., INVESTIGATING THE INVOLVEMENT OF 18Q23 IN THE ETIOLOGY OF WILLIAMS-SYNDROME, Cytogenetics and cell genetics, 65(3), 1994, pp. 162-162

Authors: JOENJE H LOTENFOE JR ARWERT F TENKATE LP
Citation: H. Joenje et al., COMPLEMENTATION TESTING AND GENETIC CLASSIFICATION OF FANCONIS ANEMIA, Lancet, 343(8901), 1994, pp. 862-862

Authors: OVERKAMP WJI ROOIMANS MA NEUTEBOOM I TELLEMAN P ARWERT F ZDZIENICKA MZ
Citation: Wji. Overkamp et al., GENETIC DIVERSITY OF MITOMYCIN C-HYPERSENSITIVE CHINESE-HAMSTER CELL MUTANTS - A NEW COMPLEMENTATION GROUP WITH CHROMOSOMAL INSTABILITY, Somatic cell and molecular genetics, 19(5), 1993, pp. 431-437

Authors: ZDZIENICKA MZ TELLEMAN P OVERKAMP WJI ARWERT F WESTERVELD A
Citation: Mz. Zdzienicka et al., CLONING OF FANCONI-ANEMIA GROUP-A GENE BY USING RODENT CELL V-H4 MUTANT, Experimental hematology, 21(5), 1993, pp. 709-710

Authors: WIJKER M WSZOLEK ZK WOLTERS ECH PALS G PFEIFFER RF RODNITZKY RL ARWERT F
Citation: M. Wijker et al., GENETIC-LINKAGE ANALYSIS IN RAPIDLY PROGRESSIVE AUTOSOMAL-DOMINANT PARKINSONISM AND DEMENTIA WITH PALLIDOPONTONIGRAL DEGENERATION (RPADP), American journal of human genetics, 53(3), 1993, pp. 1721-1721
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