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Results: 1-13 |
Results: 13
LIPOPHILICITY OF SULFUR-CONTAINING TOXIN IS A FUNDAMENTAL CRITERION IN UNDERSTANDING CHEMICAL DECONTAMINATION BY ORGANIZED MEDIA
Authors: GONZAGA F SEGUES B PEREZ E RICOLATTES I LATTES A
Citation: F. Gonzaga et al., LIPOPHILICITY OF SULFUR-CONTAINING TOXIN IS A FUNDAMENTAL CRITERION IN UNDERSTANDING CHEMICAL DECONTAMINATION BY ORGANIZED MEDIA, COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE, 1(3), 1998, pp. 209-216
NOVEL INTRAGENIC DELETIONS AND POINT MUTATIONS OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA
Authors: CALVAS P SEGUES B ROZET JM RABIER D BONNEFOND JP MUNNICH A
Citation: P. Calvas et al., NOVEL INTRAGENIC DELETIONS AND POINT MUTATIONS OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA, Human mutation, 1998, pp. 81-84
SEVERE MANIFESTATIONS IN CARRIER FEMALES AT THE RP3 LOCUS IN X-LINKEDRETINITIS-PIGMENTOSA
Authors: SOUIED EH ROZET JM SEGUES B GHAZI I GERBER S PERRAULT I CHATELIN S SOUBRANE G COSCAS G DUFFIER JL MUNNICH A KAPLAN J
Citation: Eh. Souied et al., SEVERE MANIFESTATIONS IN CARRIER FEMALES AT THE RP3 LOCUS IN X-LINKEDRETINITIS-PIGMENTOSA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3696-3696
SEVERE MANIFESTATIONS IN CARRIER FEMALES IN X-LINKED RETINITIS-PIGMENTOSA
Authors: SOUIED E SEGUES B GHAZI I ROZET JM CHATELIN S GERBER S PERRAULT I MICHELAWAD A BRIARD ML PLESSIS G DUFIER JL MUNNICH A KAPLAN J
Citation: E. Souied et al., SEVERE MANIFESTATIONS IN CARRIER FEMALES IN X-LINKED RETINITIS-PIGMENTOSA, Journal of Medical Genetics, 34(10), 1997, pp. 793-797
SEVERE MANIFESTATIONS IN CARRIER FEMALES AT THE RP3 LOCUS IN X-LINKEDRETINITIS-PIGMENTOSA
Authors: KAPLAN J SOUIED E ROZET JM SEGUES B GHAZI I GERBER S PERRAULT I CHATELIN S DUFIER JL MUNNICH A
Citation: J. Kaplan et al., SEVERE MANIFESTATIONS IN CARRIER FEMALES AT THE RP3 LOCUS IN X-LINKEDRETINITIS-PIGMENTOSA, American journal of human genetics, 61(4), 1997, pp. 1967-1967
A 3-BASE PAIR IN-FRAME DELETION IN EXON-8 (DELGLU272 273) OF THE ORNITHINE TRANSCARBAMYLASE GENE IN LATE-ONSET HYPERAMMONEMIC COMA/
Authors: SEGUES B VEBER PS RABIER D CALVAS P SAUDUBRAY JM GILBERTDUSSARDIER B BONNEFONT JP MUNNICH A
Citation: B. Segues et al., A 3-BASE PAIR IN-FRAME DELETION IN EXON-8 (DELGLU272 273) OF THE ORNITHINE TRANSCARBAMYLASE GENE IN LATE-ONSET HYPERAMMONEMIC COMA/, Human mutation, 8(4), 1996, pp. 373-374
PARTIAL DUPLICATION [DUP-TCAC-(178)] AND NOVEL POINT MUTATIONS (T125M, G188R, A209V, AND H302L) OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA
Authors: GILBERTDUSSARDIER B SEGUES B ROZET JM RABIER D CALVAS P DELUMLEY L BONNEFOND JP MUNNICH A
Citation: B. Gilbertdussardier et al., PARTIAL DUPLICATION [DUP-TCAC-(178)] AND NOVEL POINT MUTATIONS (T125M, G188R, A209V, AND H302L) OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA, Human mutation, 8(1), 1996, pp. 74-76
CHEMICAL DECONTAMINATION .1. DEPHOSPHORYL ATION OF ORGANOPHOSPHORUS COMPOUNDS
Authors: SEGUES B PEREZ E RICOLATTES I RIVIERE M LATTES A
Citation: B. Segues et al., CHEMICAL DECONTAMINATION .1. DEPHOSPHORYL ATION OF ORGANOPHOSPHORUS COMPOUNDS, Bulletin de la Societe chimique de France, 133(10), 1996, pp. 925-937
APPARENT SEGREGATION OF NULL ALLELES ASCRIBED TO DELETIONS OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA
Authors: SEGUES B ROZET JM GILBERT B SAUGIERVEBER P RABIER D SAUDUBRAY JM CARRE M ROULEAU FP MENGET A BONARDI JM LYONNET S BONNEFONT JP MUNNICH A
Citation: B. Segues et al., APPARENT SEGREGATION OF NULL ALLELES ASCRIBED TO DELETIONS OF THE ORNITHINE TRANSCARBAMYLASE GENE IN CONGENITAL HYPERAMMONEMIA, Prenatal diagnosis, 15(8), 1995, pp. 757-761
LDL-LINKED LARIAT-BEARING CYCLOPHOSPHAZENES - AN ATTEMPT AT THE PRODUCTION OF PRECURSORS FOR NEW WATER-SOLUBLE MAGNETIC-RESONANCE-IMAGING AGENTS
Authors: SEGUES B SOURNIES F CRASNIER F LABARRE JF
Citation: B. Segues et al., LDL-LINKED LARIAT-BEARING CYCLOPHOSPHAZENES - AN ATTEMPT AT THE PRODUCTION OF PRECURSORS FOR NEW WATER-SOLUBLE MAGNETIC-RESONANCE-IMAGING AGENTS, Phosphorus, sulfur and silicon and the related elements, 88(1-4), 1994, pp. 123-127
DRY MEDIA PROCESS - A CHEMAC (CHEMICAL MACHINERY) FOR THE AMINOLYSIS OF HEXACHLOROCYCLOTRIPHOSPHAZENE ON SOLID SUPPORTS
Authors: SOURNIES F GRAFFEUIL M SEGUES B CRASNIER F SEMENZIN D ETEMADMOGHADAM G KOENIG M LABARRE JF
Citation: F. Sournies et al., DRY MEDIA PROCESS - A CHEMAC (CHEMICAL MACHINERY) FOR THE AMINOLYSIS OF HEXACHLOROCYCLOTRIPHOSPHAZENE ON SOLID SUPPORTS, Phosphorus, sulfur and silicon and the related elements, 86(1-4), 1994, pp. 1-12
A NOVEL ARGININE-(245) TO GLUTAMINE CHANGE IN EXON-8 OF THE ORNITHINECARBAMOYL TRANSFERASE GENE IN 2 UNRELATED CHILDREN PRESENTING WITH LATE-ONSET DEFICIENCY AND SHOWING THE SAME ENZYMATIC PATTERN
Authors: GILBERTDUSSARDIER B RABIER D STRAUTNIEKS S SEGUES B BONNEFONT JP MUNNICH A
Citation: B. Gilbertdussardier et al., A NOVEL ARGININE-(245) TO GLUTAMINE CHANGE IN EXON-8 OF THE ORNITHINECARBAMOYL TRANSFERASE GENE IN 2 UNRELATED CHILDREN PRESENTING WITH LATE-ONSET DEFICIENCY AND SHOWING THE SAME ENZYMATIC PATTERN, Human molecular genetics, 3(5), 1994, pp. 831-832
PRENATAL-DIAGNOSIS AND GENETIC-COUNSELING IN ORNITHINE TRANSCARBAMYLASE DEFICIENCY
Authors: ROZET JM PELET A RABIER D SEGUES B SAUGIER P LYONNET S BONAITI C SAUDUBRAY JM KAMOUN P MUNNICH A
Citation: Jm. Rozet et al., PRENATAL-DIAGNOSIS AND GENETIC-COUNSELING IN ORNITHINE TRANSCARBAMYLASE DEFICIENCY, Annales de biologie clinique, 51(3-5), 1993, pp. 296-296
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