Authors:
REITER LT
HASTINGS PJ
NELIS E
DEJONGHE P
VANBROECKHOVEN C
LUPSKI JR
Citation: Lt. Reiter et al., HUMAN MEIOTIC RECOMBINATION PRODUCTS REVEALED BY SEQUENCING A HOTSPOTFOR HOMOLOGOUS STRAND EXCHANGE IN MULTIPLE HNPP DELETION PATIENTS, American journal of human genetics, 62(5), 1998, pp. 1023-1033
Authors:
BEUTEN J
DEJONGHE P
CEUTERICK C
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: J. Beuten et al., CONSTRUCTION OF A YAC CONTIG OF THE DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II REGION AT 12Q24, European journal of neuroscience, 10, 1998, pp. 15901-15901
Authors:
NELIS E
DEJONGHE P
DEVRIENDT E
PATEL PI
MARTIN JJ
VANBROECKHOVEN C
Citation: E. Nelis et al., MUTATION ANALYSIS OF THE NERVE SPECIFIC PROMOTER OF THE PERIPHERAL MYELIN PROTEIN-22 GENE IN CMT1 DISEASE AND HNPP, Journal of Medical Genetics, 35(7), 1998, pp. 590-593
Authors:
NELIS E
SIMOKOVIC S
TIMMERMAN V
LOFGREN A
BACKHOVENS H
DEJONGHE P
MARTIN JJ
VANBROECKHOVEN C
Citation: E. Nelis et al., MUTATION ANALYSIS OF THE CONNEXIN-32 (CX32) GENE IN CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1 - IDENTIFICATION OF 5 NEW MUTATIONS, Human mutation, 9(1), 1997, pp. 47-52
Authors:
BEUTEN J
DEVRIENDT E
DEJONGHE P
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: J. Beuten et al., MUTATION ANALYSIS OF THE HUMAN PANCREATIC PHOSPHOLIPASE A(2) GENE IN A FAMILY WITH DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II LINKED TO 12Q24, Neuroscience letters, 223(1), 1997, pp. 69-71
Authors:
TIMMERMAN V
BEUTEN J
DEJONGHE P
MARTIN JJ
VANBROECKHOVEN C
Citation: V. Timmerman et al., ASSIGNMENT OF THE LOCUS FOR DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II (DISTAL HMN-II) TO CHROMOSOME-12Q24, Acta neurologica belgica, 97(1), 1997, pp. 56-56
Authors:
DEJONGHE P
TIMMERMAN V
FITZPATRICK D
SPOELDERS P
MARTIN JJ
VANBROECKHOVEN C
Citation: P. Dejonghe et al., MUTILATING NEUROPATHIC ULCERATIONS IN A CHROMOSOME 3Q13-Q22 LINKED CHARCOT-MARIE-TOOTH DISEASE TYPE 2B FAMILY, Journal of Neurology, Neurosurgery and Psychiatry, 62(6), 1997, pp. 570-573
Authors:
TIMMERMAN V
RAUTENSTRAUSS B
REITER LT
KOEUTH T
LOFGREN A
LIEHR T
NELIS E
BATHKE KD
DEJONGHE P
GREHL H
MARTIN JJ
LUPSKI JR
VANBROECKHOVEN C
Citation: V. Timmerman et al., DETECTION OF THE CMT1A HNPP RECOMBINATION HOTSPOT IN UNRELATED PATIENTS OF EUROPEAN DESCENT/, Journal of Medical Genetics, 34(1), 1997, pp. 43-49
Authors:
BEUTEN J
DEJONGHE P
CEUTERICK C
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: J. Beuten et al., CONSTRUCTION OF A YAC CONTIG OF THE 12Q24 REGION FOR THE FINE MAPPINGOF A LOCUS FOR DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II, American journal of human genetics, 61(4), 1997, pp. 1343-1343
Authors:
TIMMERMAN V
DEJONGHE P
DEVRIENDT E
FITZPATRICK D
MALCOLM S
VANBROECKHOVEN C
Citation: V. Timmerman et al., GENETIC-LINKAGE ANALYSIS IN FAMILIES WITH CHARCOT-MARIE-TOOTH TYPE-2 NEUROPATHY, American journal of human genetics, 61(4), 1997, pp. 2358-2358
Authors:
SPOELDERS P
LOFGREN A
DEJONGHE P
NELIS E
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: P. Spoelders et al., MOLECULAR-GENETIC ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2 (CMT2) FAMILIES WITH CHROMOSOME 1P35-36 AND 3Q13-22 MARKERS, Archives of physiology and biochemistry, 104(3), 1996, pp. 51-51
Authors:
DEJONGHE P
KROLS L
MICHALIK A
HAZAN J
SMEYERS G
LOFGREN A
WEISSENBACH J
MARTIN JJ
VANBROECKHOVEN C
Citation: P. Dejonghe et al., PURE FAMILIAL SPASTIC PARAPLEGIA - CLINICAL AND GENETIC-ANALYSIS OF 9BELGIAN PEDIGREES, European journal of human genetics, 4(5), 1996, pp. 260-266
Authors:
TIMMERMAN V
DEJONGHE P
SIMOKOVIC S
LOFGREN A
BEUTEN J
NELIS E
CEUTERICK C
MARTIN JJ
VANBROECKHOVEN C
Citation: V. Timmerman et al., DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II (DISTAL HMN-II) - MAPPING OF A LOCUS TO CHROMOSOME 12Q24, Human molecular genetics, 5(7), 1996, pp. 1065-1069
Authors:
TIMMERMAN V
LOFGREN A
LEGUERN E
LIANG P
DEJONGHE P
MARTIN JJ
VERHALLE D
ROBBERECHT W
GOUIDER R
BRICE A
VANBROECKHOVEN C
Citation: V. Timmerman et al., MOLECULAR-GENETIC ANALYSIS OF THE 17P11.2 REGION IN PATIENTS WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP), Human genetics, 97(1), 1996, pp. 26-34
Authors:
KROLS L
MICHALIK A
DEJONGHE P
MARTIN JJ
VANBROECKHOVEN C
Citation: L. Krols et al., YAC CONTIG MAP OF THE CANDIDATE REGION FOR FAMILIAL SPASTIC PARAPLEGIA (SPG4) ON CHROMOSOME 2P21-]P14, Cytogenetics and cell genetics, 73(4), 1996, pp. 7-7
Authors:
TIMMERMAN V
DEJONGHE P
SPOELDERS P
SIMOKOVIC S
LOFGREN A
NELIS E
VANCE J
MARTIN JJ
VANBROECKHOVEN C
Citation: V. Timmerman et al., LINKAGE AND MUTATION ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2 FAMILIES WITH CHROMOSOMES 1P35-P36 AND XQ13, Neurology, 46(5), 1996, pp. 1311-1318
Authors:
NELIS E
TIMMERMAN V
DEJONGHE P
VANBROECKHOVEN C
Citation: E. Nelis et al., IDENTIFICATION OF A 5' SPLICE-SITE MUTATION IN THE PMP-22 GENE IN AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-1, Human molecular genetics, 3(3), 1994, pp. 515-516
Authors:
NELIS E
TIMMERMAN V
DEJONGHE P
VANDENBERGHE A
PHAMDINH D
DAUTIGNY A
MARTIN JJ
VANBROECKHOVEN C
Citation: E. Nelis et al., RAPID SCREENING OF MYELIN GENES IN CMT1 PATIENTS BY SSCP ANALYSIS - IDENTIFICATION OF NEW MUTATIONS AND POLYMORPHISMS IN THE P-0 GENE, Human genetics, 94(6), 1994, pp. 653-657
Authors:
NELIS E
TIMMERMAN V
DEJONGHE P
MUYLLE L
MARTIN JJ
VANBROECKHOVEN C
Citation: E. Nelis et al., LINKAGE AND MUTATION ANALYSIS IN AN EXTENDED FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B, Journal of Medical Genetics, 31(10), 1994, pp. 811-815
Authors:
PALAU F
LOFGREN A
DEJONGHE P
BORT S
NELIS E
SEVILLA T
MARTIN JJ
VILCHEZ J
PRIETO F
VANBROECKHOVEN C
Citation: F. Palau et al., ORIGIN OF THE DE-NOVO DUPLICATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE1A - UNEQUAL NONSISTER CHROMATID EXCHANGE DURING SPERMATOGENESIS, Human molecular genetics, 2(12), 1993, pp. 2031-2035