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Results: 1-6 |
Results: 6

Authors: VERZIJL HTFM VANENGELEN BGM LUYTEN JAFM STEENBERGEN GCH VANDENHEUVEL LPWJ TERLAAK HJ PADBERG GW WEVERS RA
Citation: Htfm. Verzijl et al., GENETIC-CHARACTERISTICS OF MYOADENYLATE DEAMINASE DEFICIENCY, Annals of neurology, 44(1), 1998, pp. 140-143

Authors: WIJMENGA C VANDENHEUVEL LPWJ STRENGMAN E LUYTEN JAFM VANDERBURGT IJAM DEGROOT R SMEETS DFCM DRAAISMA JMT VANDONGEN JJ DEABREU RA PEARSON PL SANDKUIJL LA WEEMAES CMR
Citation: C. Wijmenga et al., LOCALIZATION OF THE ICF SYNDROME TO CHROMOSOME-20 BY HOMOZYGOSITY MAPPING, American journal of human genetics, 63(3), 1998, pp. 803-809

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM WEVERS RA WOKKE JHJ GABREELS FJM WOLTHERS BG VANDENHEUVEL LPWJ
Citation: A. Verrips et al., EXON SKIPPING IN THE STEROL 27-HYDROXYLASE GENE LEADS TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 100(2), 1997, pp. 284-286

Authors: VERRIPS A STEENBERGENSPANJERS GCH LUYTEN JAFM VANDENHEUVEL LPWJ KEYSER A GABREELS FJM WEVERS RA
Citation: A. Verrips et al., 2 NEW MUTATIONS IN THE STEROL 27-HYDROXYLASE GENE IN 2 FAMILIES LEAD TO CEREBROTENDINOUS XANTHOMATOSIS, Human genetics, 98(6), 1996, pp. 735-737

Authors: LUYTEN JAFM WENINK PW STEENBERGENSPANJERS GCH WEVERS RA VANAMSTEL HKP DEJONG JGN VANDENHEUVEL LPWJ
Citation: Jafm. Luyten et al., METACHROMATIC LEUKODYSTROPHY - A 12-BP DELETION IN EXON-2 OF THE ARYLSULFATASE-A GENE IN A LATE INFANTILE VARIANT, Human genetics, 96(3), 1995, pp. 357-360

Authors: LINN FHH LUYTEN JAFM VANGIJN J JANSEN GH
Citation: Fhh. Linn et al., PRIMARY PROGRESSIVE HEMIPARESIS, Journal of Neurology, Neurosurgery and Psychiatry, 59(3), 1995, pp. 339-340
Risultati: 1-6 |