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Results: 1-12 |
Results: 12
GENOMIC STRUCTURE AND PHYSICAL MAPPING OF C17ORF1 - A GENE ASSOCIATEDWITH THE PROXIMAL ELEMENT OF THE CMT1A-REP BINARY REPEAT
Authors: KENNERSON ML NASSIF NT NICHOLSON GA
Citation: Ml. Kennerson et al., GENOMIC STRUCTURE AND PHYSICAL MAPPING OF C17ORF1 - A GENE ASSOCIATEDWITH THE PROXIMAL ELEMENT OF THE CMT1A-REP BINARY REPEAT, Genomics (San Diego, Calif.), 53(1), 1998, pp. 110-112
THE CHARCOT-MARIE-TOOTH BINARY REPEAT CONTAINS A GENE TRANSCRIBED FROM THE OPPOSITE STRAND OF A PARTIALLY DUPLICATED REGION OF THE COX10 GENE
Authors: KENNERSON ML NASSIF NT DAWKINS JL DEKROON RM YANG JG NICHOLSON GA
Citation: Ml. Kennerson et al., THE CHARCOT-MARIE-TOOTH BINARY REPEAT CONTAINS A GENE TRANSCRIBED FROM THE OPPOSITE STRAND OF A PARTIALLY DUPLICATED REGION OF THE COX10 GENE, Genomics, 46(1), 1997, pp. 61-69
THE GENE FOR HEREDITARY SENSORY NEUROPATHY TYPE-I (HSN-I) MAPS TO CHROMOSOME 9Q22.1-Q22.3
Authors: NICHOLSON GA DAWKINS JL BLAIR IP KENNERSON ML GORDON MJ CHERRYSON AK NASH A BANANIS T
Citation: Ga. Nicholson et al., THE GENE FOR HEREDITARY SENSORY NEUROPATHY TYPE-I (HSN-I) MAPS TO CHROMOSOME 9Q22.1-Q22.3, Nature genetics, 13(1), 1996, pp. 101-104
DETECTION OF CHARCOT-MARIE-TOOTH TYPE 1A DUPLICATION BY THE POLYMERASE CHAIN-REACTION
Authors: BLAIR IP KENNERSON ML NICHOLSON GA
Citation: Ip. Blair et al., DETECTION OF CHARCOT-MARIE-TOOTH TYPE 1A DUPLICATION BY THE POLYMERASE CHAIN-REACTION, Clinical chemistry, 41(8), 1995, pp. 1105-1108
SINGLE TEST FOR 2 HEREDITARY NEUROPATHIES, CMT1A AND HNPP
Authors: KENNERSON ML GORDON MJ BLAIR IP NICHOLSON GA
Citation: Ml. Kennerson et al., SINGLE TEST FOR 2 HEREDITARY NEUROPATHIES, CMT1A AND HNPP, Clinical chemistry, 41(10), 1995, pp. 1534-1535
NOVEL GENES IN THE CMT1A-ASSOCIATED DNA DUPLICATION ON CHROMOSOME 17P11.2 IDENTIFIED BY EXON AMPLIFICATION
Authors: MEIJERINK PHS ZORN I KENNERSON ML ROSS DA NICHOLSON GA BOLHUIS PA BAAS F
Citation: Phs. Meijerink et al., NOVEL GENES IN THE CMT1A-ASSOCIATED DNA DUPLICATION ON CHROMOSOME 17P11.2 IDENTIFIED BY EXON AMPLIFICATION, American journal of human genetics, 57(4), 1995, pp. 1536-1536
CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1
Authors: PERICAKVANCE MA BARKER DF BERGOFFEN JA CHANCE P COCHRANE S DAHL N EXLER MC FAIN PR FAIRWEATHER ND FISCHBECK K GAL A HAITES N IONASESCU R IONASESCU VV KENNERSON ML MONACO AP MOSTACCUIOLO M NICHOLSON GA SILLEN A HAINES JL
Citation: Ma. Pericakvance et al., CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1, Human heredity, 45(3), 1995, pp. 121-128
A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (VOL 6, PG 263, 1994)
Authors: NICHOLSON GA VALENTIJN LJ CHERRYSON AK KENNERSON ML BRAGG TL DEKROON RM ROSS DA POLLARD JD MCLEOD JG BOLHUIS PA BAAS F
Citation: Ga. Nicholson et al., A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (VOL 6, PG 263, 1994), Nature genetics, 7(1), 1994, pp. 113-113
A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: NICHOLSON GA VALENTIJN LJ CHERRYSON AK KENNERSON ML BRAGG TL DEKROON RM ROSS DA POLLARD JD MCLEOD JG BOLHUIS PA BAAS F
Citation: Ga. Nicholson et al., A FRAME-SHIFT MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Nature genetics, 6(3), 1994, pp. 263-266
PHENOTYPIC-EXPRESSION OF BENIGN FAMILIAL NEONATAL CONVULSIONS LINKED TO CHROMOSOME-20
Authors: BERKOVIC SF KENNERSON ML HOWELL RA SCHEFFER IE HWANG PA NICHOLSON GA
Citation: Sf. Berkovic et al., PHENOTYPIC-EXPRESSION OF BENIGN FAMILIAL NEONATAL CONVULSIONS LINKED TO CHROMOSOME-20, Archives of neurology, 51(11), 1994, pp. 1125-1128
MOLECULAR ANALYSIS OF DELETED AND NON-DELETED HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY (HNPP) FAMILIES
Authors: KENNERSON ML ROSS DA NICHOLSON GA
Citation: Ml. Kennerson et al., MOLECULAR ANALYSIS OF DELETED AND NON-DELETED HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY (HNPP) FAMILIES, American journal of human genetics, 53(3), 1993, pp. 1182-1182
IDENTIFICATION OF 14 POTENTIAL GENE-SEQUENCES (HTF ISLANDS) IN THE CMT1A DUPLICATION HNPP DELETION AREA
Authors: ROSS DA KENNERSON ML NICHOLSON GA
Citation: Da. Ross et al., IDENTIFICATION OF 14 POTENTIAL GENE-SEQUENCES (HTF ISLANDS) IN THE CMT1A DUPLICATION HNPP DELETION AREA, American journal of human genetics, 53(3), 1993, pp. 1351-1351
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