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Authors: YAMAMOTO M KELLER MP YASUDA T HAYASAKA K OHNISHI A YOSHIKAWA H YANAGIHARA T MITSUMA T CHANCE PF SOBUE G
Citation: M. Yamamoto et al., CLUSTERING OF CMT1A DUPLICATION BREAKPOINTS IN A 700 BP INTERVAL OF THE CMT1A-REP REPEAT, Human mutation, 11(2), 1998, pp. 109-113

Authors: RABIN BA GRIFFIN JW CRAIN BJ SCAVINA M CHANCE PF CORNBLATH DR
Citation: Ba. Rabin et al., NEUROPATHOLOGY OF AUTOSOMAL-DOMINANT JUVENILE AMYOTROPHIC-LATERAL-SCLEROSIS, Annals of neurology, 44(3), 1998, pp. 138-138

Authors: GOSSETT JG CHANCE PF
Citation: Jg. Gossett et Pf. Chance, IS THERE A FAMILIAL CARPAL-TUNNEL SYNDROME - AN EVALUATION AND LITERATURE-REVIEW, Muscle & nerve, 21(11), 1998, pp. 1533-1536

Authors: CHANCE PF DYCK PJ
Citation: Pf. Chance et Pj. Dyck, HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - A PATIENTSPOINT MUTATION IN A MOUSE MODEL, Neurology, 51(3), 1998, pp. 664-665

Authors: CHANCE PF
Citation: Pf. Chance, GENETIC-LINKAGE ANALYSIS AS A TOOL FOR UNDERSTANDING THE MOLECULAR-BASIS OF HUMAN-DISEASE, Journal of neurochemistry, 70, 1998, pp. 78-78

Authors: CHANCE PF RABIN BA RYAN SG DING Y SCAVINA M CONWAY D CRAIN B GRIFFIN JW CORNBLATH DR
Citation: Pf. Chance et al., LINKAGE OF THE GENE FOR AN AUTOSOMAL-DOMINANT FORM OF JUVENILE AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 9Q34 (VOL 62, PG 633, 1998), American journal of human genetics, 63(1), 1998, pp. 295-295

Authors: CHANCE PF RABIN BA RYAN SG DING Y SCAVINA M CRAIN B GRIFFIN JW CORNBLATH DR
Citation: Pf. Chance et al., LINKAGE OF THE GENE FOR AN AUTOSOMAL-DOMINANT FORM OF JUVENILE AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 9Q34, American journal of human genetics, 62(3), 1998, pp. 633-640

Authors: RYAN SG CHANCE PF ZOU CH SPINNER NB GOLDEN JA SMIETANA S
Citation: Sg. Ryan et al., EPILEPSY AND MENTAL-RETARDATION LIMITED TO FEMALES - AN X-LINKED DOMINANT DISORDER WITH MALE SPARING, Nature genetics, 17(1), 1997, pp. 92-95

Authors: RYAN SG CHANCE PF GOLDEN JA SMIETANA S
Citation: Sg. Ryan et al., A FAMILY WITH EPILEPSY AND MENTAL-RETARDATION LIMITED TO FEMALES DEFINES A NEW INHERITANCE PATTERN - X-LINKAGE WITH MALE SPARING, Annals of neurology, 42(3), 1997, pp. 1-1

Authors: YAMAMOTO M YASUDA T HAYASAKA K OHNISHI A YOSHIKAWA H YANAGIHARA T IKEGAMI T YAMAMOTO T OHASHI H NISHIMURA T MITSUMA T KIYOSAWA H CHANCE PF SOBUE G
Citation: M. Yamamoto et al., LOCATIONS OF CROSSOVER BREAKPOINTS WITHIN THE CMT1A-REP REPEAT IN JAPANESE PATIENTS WITH CMT1A AND HNPP, Human genetics, 99(2), 1997, pp. 151-154

Authors: PELLEGRINO JE GEORGE RAV BIEGEL J FARLOW MR GARDNER K CARESS J BROWN MJ REBBECK TR BIRD TD CHANCE PF
Citation: Je. Pellegrino et al., HEREDITARY NEURALGIC AMYOTROPHY - EVIDENCE FOR GENETIC HOMOGENEITY AND MAPPING TO CHROMOSOME 17Q25, Human genetics, 101(3), 1997, pp. 277-283

Authors: PELLEGRINO JE LENSCH MW MUENKE M CHANCE PF
Citation: Je. Pellegrino et al., CLINICAL AND MOLECULAR ANALYSIS IN JOUBERT-SYNDROME, American journal of medical genetics, 72(1), 1997, pp. 59-62

Authors: VADASZ AG CHANCE PF EPSTEIN LG LOU JS
Citation: Ag. Vadasz et al., FAMILIAL AUTOSOMAL-DOMINANT CARPAL-TUNNEL SYNDROME PRESENTING IN A 5-YEAR-OLD CASE-REPORT AND REVIEW OF THE LITERATURE, Muscle & nerve, 20(3), 1997, pp. 376-378

Authors: LYNCH DR HARA H YUM SW CHANCE PF SCHERER SS BIRD SJ FISCHBECK KH
Citation: Dr. Lynch et al., AUTOSOMAL-DOMINANT TRANSMISSION OF DEJERINE-SOTTAS-DISEASE (HMSN-III), Neurology, 49(2), 1997, pp. 601-603

Authors: KELLER MP CHANCE PF
Citation: Mp. Keller et Pf. Chance, CMT1A-REP REPEAT - MOLECULAR ONTOGENY AND FURTHER DEFINITION OF A RECOMBINATIONAL HOTSPOT, American journal of human genetics, 61(4), 1997, pp. 1168-1168

Authors: PELLEGRINO JE GEORGE RAV BIEGEL J FARLOW MR GARDNER K CARESS J BROWN MJ REBBECK TR BIRD TD CHANCE PF
Citation: Je. Pellegrino et al., HEREDITARY NEURALGIC AMYOTROPHY - REFINED MAPPING TO CHROMOSOME 17Q25, American journal of human genetics, 61(4), 1997, pp. 1694-1694

Authors: CHANCE PF WINDEBANK AJ
Citation: Pf. Chance et Aj. Windebank, HEREDITARY NEURALGIC AMYOTROPHY, Current opinion in neurology, 9(5), 1996, pp. 343-347

Authors: ROA BB WARNER LE GARCIA CA RUSSO D LOVELACE R CHANCE PF LUPSKI JR
Citation: Bb. Roa et al., MYELIN PROTEIN ZERO (MPZ) GENE-MUTATIONS IN NONDUPLICATION TYPE-1 CHARCOT-MARIE-TOOTH DISEASE, Human mutation, 7(1), 1996, pp. 36-45

Authors: NELIS E WARNER LE DEVRIENDT E CHANCE PF LUPSKI JR VANBROECKHOVEN C
Citation: E. Nelis et al., COMPARISON OF SINGLE-STRAND CONFORMATION POLYMORPHISM AND HETERODUPLEX ANALYSIS FOR DETECTION OF MUTATIONS IN CHARCOT-MARIE-TOOTH TYPE-1 DISEASE AND RELATED PERIPHERAL NEUROPATHIES, European journal of human genetics, 4(6), 1996, pp. 329-333

Authors: BINGHAM PM SPINNER NB SOVINSKY L ZACKAI EH CHANCE PF
Citation: Pm. Bingham et al., INFANTILE SPASMS ASSOCIATED WITH PROXIMAL DUPLICATION OF CHROMOSOME 15Q, Pediatric neurology, 15(2), 1996, pp. 163-165

Authors: ALLEN TL BROTHMAN AR CAREY JC CHANCE PF
Citation: Tl. Allen et al., CYTOGENETIC AND MOLECULAR ANALYSIS IN TRISOMY 12P, American journal of medical genetics, 63(1), 1996, pp. 250-256

Authors: PELLEGRINO JE REBBECK TR BROWN MJ BIRD TD CHANCE PF
Citation: Je. Pellegrino et al., MAPPING OF HEREDITARY NEURALGIC AMYOTROPHY (FAMILIAL BRACHIAL-PLEXUS NEUROPATHY) TO DISTAL CHROMOSOME 17Q, Neurology, 46(4), 1996, pp. 1128-1132

Authors: PELLEGRINO JE REBBECK TR BROWN MJ FARLOW MR BROWN RH BUSIS NA CARESS J LIPE H BIRD TD CHANCE PF
Citation: Je. Pellegrino et al., GENETIC-ANALYSIS IN HEREDITARY NEURALGIC AMYOTROPHY, Neurology, 46(2), 1996, pp. 21001-21001

Authors: GROSS DW RAJPUT AH CHANCE PF YEUNG M
Citation: Dw. Gross et al., HEREDITARY DISTAL ULNAR-MEDIAN MUSCULAR-ATROPHY - A DISTINCT INHERITED MOTOR NEUROPATHY, Neurology, 46(2), 1996, pp. 35002-35002

Authors: YOSHIOKA R DYCK PJ CHANCE PF
Citation: R. Yoshioka et al., GENETIC-HETEROGENEITY IN CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2, Neurology, 46(2), 1996, pp. 569-571
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