Authors: ELMSLIE FV REES M WILLIAMSON MP KERR M KJELDSEN MJ PANG KA SUNDQVIST A FRIIS ML CHADWICK D RICHENS A COVANIS A SANTOS M ARZIMANOGLOU A PANAYIOTOPOULOS CP CURTIS D WHITEHOUSE WP GARDINER RM

Citation: Fv. Elmslie et al., GENETIC-MAPPING OF A MAJOR SUSCEPTIBILITY LOCUS FOR JUVENILE MYOCLONIC EPILEPSY ON CHROMOSOME 15Q, Human molecular genetics, 6(8), 1997, pp. 1329-1334

Authors: ELMSLIE FV WILLIAMSON MP REES M KERR M KJELDSEN MJ PANG KA SUNDQVIST A FRIIS ML RICHENS A CHADWICK D WHITEHOUSE WP GARDINER RM

Citation: Fv. Elmslie et al., LINKAGE ANALYSIS OF JUVENILE MYOCLONIC EPILEPSY AND MICROSATELLITE LOCI SPANNING 61 CM OF HUMAN-CHROMOSOME 6P IN 19 NUCLEAR PEDIGREES PROVIDES NO EVIDENCE FOR A SUSCEPTIBILITY LOCUS IN THIS REGION, American journal of human genetics, 59(3), 1996, pp. 653-663

Authors: REES M CURTIS D PARKER K SUNDQVIST A BARALLE D BESPALOVA IN BURMEISTER M CHUNG E GARDINER RM WHITEHOUSE WP

Citation: M. Rees et al., LINKAGE ANALYSIS OF IDIOPATHIC GENERALIZED EPILEPSY IN FAMILIES OF PROBANDS WITH JUVENILE MYOCLONIC EPILEPSY AND MARKER LOCI THE REGION OF EPM-1 ON CHROMOSOME 21Q - UNVERRICHT-LUNDBORG DISEASE AND JME ARE NOT ALLELIC VARIANTS, Neuropediatrics, 25(1), 1994, pp. 20-25

Authors: REES M DIEBOLD U PARKER K DOOSE H GARDINER RM WHITEHOUSE WP

Citation: M. Rees et al., BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION, Neuropediatrics, 24(4), 1993, pp. 211-213

Authors: REES M SUNDQVIST A WHITEHOUSE WP GARDINER RM

Citation: M. Rees et al., SEQUENCE-ANALYSIS OF THE HUMAN BRAIN K+ CHANNEL GENE HBK2 IN JUVENILEMYOCLONIC EPILEPSY PATIENTS, American journal of human genetics, 53(3), 1993, pp. 493-493

Authors: WHITEHOUSE WP REES M CURTIS D SUNDQVIST A PARKER K CHUNG E BARALLE D GARDINER RM

Citation: Wp. Whitehouse et al., LINKAGE ANALYSIS OF IDIOPATHIC GENERALIZED EPILEPSY (IGE) AND MARKER LOCI ON CHROMOSOME-6P IN FAMILIES OF PATIENTS WITH JUVENILE MYOCLONIC EPILEPSY - NO EVIDENCE FOR AN EPILEPSY LOCUS IN THE HLA REGION, American journal of human genetics, 53(3), 1993, pp. 652-662