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Results:
1-21
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Results: 21
Authors:
VONFELLENBERG J
PATERNOTTE C
PRUDHOMME JF
WEISSENBACH J
HAZAN J
BURGUNDER JM
Citation: J. Vonfellenberg et al., CLINICAL AND GENETIC-ANALYSIS OF 4 SWISS FAMILIES WITH THE PURE FORM OF HEREDITARY SPASTIC PARAPLEGIA, Schweizerische medizinische Wochenschrift, 128(26), 1998, pp. 1043-1050
Authors:
HEINZLEF O
PATERNOTTE C
MAHIEUX F
PRUDHOMME JF
DIEN J
MADIGAND M
POUGET J
WEISSENBACH J
ROULLET E
HAZAN J
Citation: O. Heinzlef et al., MAPPING OF A COMPLICATED FAMILIAL SPASTIC PARAPLEGIA TO LOCUS SPG4 ONCHROMOSOME 2P, Journal of Medical Genetics, 35(2), 1998, pp. 89-93
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:
VICART P
DUPRET JM
HAZAN J
LI ZL
GYAPAY G
KRISHNAMOORTHY R
WEISSENBACH J
FARDEAU M
PAULIN D
Citation: P. Vicart et al., HUMAN DESMIN GENE - CDNA SEQUENCE, REGIONAL LOCALIZATION AND EXCLUSION OF THE LOCUS IN A FAMILIAL DESMIN-RELATED MYOPATHY, Human genetics, 98(4), 1996, pp. 422-429
Authors:
BURGER J
METZKE H
PATERNOTTE C
SCHILLING F
HAZAN J
REIS A
Citation: J. Burger et al., AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA WITH ANTICIPATION MAPS TO A 4-CM INTERVAL ON CHROMOSOME 2P21-P24 IN A LARGE GERMAN FAMILY, Human genetics, 98(3), 1996, pp. 371-375
Authors:
DIB C
FAURE S
FIZAMES C
SAMSON D
DROUOT N
VIGNAL A
MILLASSEAU P
MARC S
HAZAN J
SEBOUN E
LATHROP M
GYAPAY G
MORISSETTE J
WEISSENBACH J
Citation: C. Dib et al., A COMPREHENSIVE GENETIC-MAP OF THE HUMAN GENOME BASED ON 5,264 MICROSATELLITES, Nature, 380(6570), 1996, pp. 152-154
Authors:
HAZAN J
CODDET C
Citation: J. Hazan et C. Coddet, CORROSION OF ZINC IN AN ALKALINE-SOLUTION - EFFECT OF CHROMIUM PASSIVATION TREATMENT, Journal of Applied Electrochemistry, 26(2), 1996, pp. 203-209
Authors:
DURR A
DAVOINE CS
PATERNOTTE C
VONFELLENBERG J
COGILNICEAN S
COUTINHO P
LAMY C
BOURGEOIS S
PRUDHOMME JF
PENET C
MAS JL
BURGUNDER JM
HAZAN J
WEISSENBACH J
BRICE A
FONTAINE B
Citation: A. Durr et al., PHENOTYPE OF AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-2, Brain, 119, 1996, pp. 1487-1496
Authors:
VINCENT P
PLAUCHU H
HAZAN J
FAURE S
WEISSENBACH J
GODET J
Citation: P. Vincent et al., A 3RD LOCUS FOR HEREDITARY HEMORRHAGIC TELANGIECTASIA MAPS TO CHROMOSOME 12Q (VOL 4, PG 945, 1995), Human molecular genetics, 4(7), 1995, pp. 1243-1243
Authors:
VINCENT P
PLAUCHU H
HAZAN J
FAURE S
WEISSENBACH J
GODET J
Citation: P. Vincent et al., A 3RD LOCUS FOR HEREDITARY HEMORRHAGIC TELANGIECTASIA MAPS TO CHROMOSOME 12Q, Human molecular genetics, 4(5), 1995, pp. 945-949
Authors:
FONTAINE B
RIME CS
HAZAN J
DURR A
STEVANIN G
PENET C
REBOUL J
AGID Y
LYONCAEN O
BAUMANN N
WEISSENBACH J
BRICE A
Citation: B. Fontaine et al., EXCLUSION OF THE CANDIDATE LOCUS FSP1 IN 6 FAMILIES WITH LATE-ONSET AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA, Neuromuscular disorders, 5(1), 1995, pp. 11-17
Authors:
FONTAINE B
HAZAN J
DAVOINE CS
DURR A
AGID Y
LYONCAEN O
WEISSENBACH J
BRICE A
Citation: B. Fontaine et al., LINKAGE ANALYSIS IN FAMILIES WITH AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA OF ADULT-ONSET (GREATER-THAN-OR-EQUAL-TO-25 YEARS OLD), Neurology, 45(4), 1995, pp. 452-452
Authors:
JAMES MR
RICHARD CW
SCHOTT JJ
YOUSRY C
CLARK K
BELL J
TERWILLIGER JD
HAZAN J
DUBAY C
VIGNAL A
AGRAPART M
IMAI T
NAKAMURA Y
POLYMEROPOULOS M
WEISSENBACH J
COX DR
LATHROP GM
Citation: Mr. James et al., A RADIATION HYBRID MAP OF 506 STS MARKERS SPANNING HUMAN-CHROMOSOME-11, Nature genetics, 8(1), 1994, pp. 70-76
Authors:
HAZAN J
FONTAINE B
BRUYN RPM
LAMY C
VANDEUTEKOM JCT
RIME CS
DURR A
MELKI J
LYONCAEN O
AGID Y
MUNNICH A
PADBERG GW
DERECONDO J
FRANTS RR
BRICE A
WEISSENBACH J
Citation: J. Hazan et al., LINKAGE OF A NEW LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME 2P, Human molecular genetics, 3(9), 1994, pp. 1569-1573
Authors:
DELEUZE JF
DHORNE S
HAZAN J
BORGHI E
RAYNAUD N
POLLET N
MEUNIERROTIVAL M
DESCHATRETTE J
ALAGILLE D
HADCHOUEL M
Citation: Jf. Deleuze et al., DELETED CHROMOSOME-20 FROM A PATIENT WITH ALAGILLE-SYNDROME ISOLATED IN A CELL HYBRID THROUGH LEUCINE TRANSPORT SELECTION - STUDY OF 3 CANDIDATE GENES, Mammalian genome, 5(11), 1994, pp. 663-669
Authors:
DELEUZE JF
DHORNE S
HAZAN J
BORGHI E
RAYNAUD N
POLLET N
MEUNIERROTIVAL M
DESCHATRETTE J
ALAGILLE D
HADCHOUEL M
Citation: Jf. Deleuze et al., DELETED CHROMOSOME-20 FROM A PATIENT WITH ALAGILLE-SYNDROME ISOLATED IN A CELL HYBRID THROUGH LEUCINE TRANSPORT SELECTION - STUDY OF 3 CANDIDATE GENES, Mammalian genome, 5(11), 1994, pp. 663-669
Authors:
JURADO LAP
PHILLIPS JA
SUMMAR ML
MAO J
WEBER JL
SCHAEFER FV
HAZAN J
ARGENTE J
Citation: Lap. Jurado et al., GENETIC-MAPPING OF THE HUMAN GROWTH HORMONE-RELEASING FACTOR GENE (GHRF) USING 2 INTRAGENIC POLYMORPHISMS DETECTED BY PCR AMPLIFICATION, Genomics, 20(1), 1994, pp. 132-134
Authors:
SMITH CL
KEITH T
HANSMANN I
WEISSENBACH J
ASIMAKOPOULOS FA
BOWDEN DW
DELEUZE JF
DUTTON ER
FASMAN KH
GREEN T
HADCHOUEL M
HAZAN J
HILGARTNER S
KINGSBURY DK
LODER B
MALAFOSSE A
MEUNIERROTIVAL M
PEARSON PL
SIRACUSA LD
STEINLEIN O
WHITE N
WILLIAMSON CM
Citation: Cl. Smith et al., REPORT OF THE FIRST ERNATIONAL-WORKSHOP-ON-HUMAN-CHROMOSOME-20-MAPPING 1993 HELD ON SEPTEMBER 6-8, 1993 AT GIF-SUR-YVETTE, FRANCE, Cytogenetics and cell genetics, 66(2), 1994, pp. 77-82
Authors:
BRICE A
RIME CS
DURR A
HAZAN J
LYONCAEN O
AGID Y
WEISSENBACH J
FONTAINE B
Citation: A. Brice et al., FSP1 (AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA OF EARLY-ONSET) IS NOT A MAJOR LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA OF LATE-ONSET, Neurology, 44(4), 1994, pp. 10000294-10000294
Authors:
HAZAN J
LAMY C
MELKI J
MUNNICH A
DERECONDO J
WEISSENBACH J
Citation: J. Hazan et al., AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA IS GENETICALLY HETEROGENEOUS AND ONE LOCUS MAPS TO CHROMOSOME-14Q, Nature genetics, 5(2), 1993, pp. 163-167
Authors:
HAZAN J
YAHALOM J
Citation: J. Hazan et J. Yahalom, CORROSION OF PROTECTED ALUMINUM AND ZINC, Corrosion science, 35(1-4), 1993, pp. 223-229
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1-21
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