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Results: 1-16 |
Results: 16
REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF ENOXACIN AND 4-OXO-ENOXACIN IN HUMAN PLASMA AND PROSTATIC TISSUE - APPLICATION TO A PHARMACOKINETIC STUDY
Authors: HAMEL B AUDRAN M COSTA P BRESSOLLE F
Citation: B. Hamel et al., REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF ENOXACIN AND 4-OXO-ENOXACIN IN HUMAN PLASMA AND PROSTATIC TISSUE - APPLICATION TO A PHARMACOKINETIC STUDY, Journal of chromatography, 812(1-2), 1998, pp. 369-379
OLIGOPHRENIN-1 ENCODES A RHOGAP PROTEIN INVOLVED IN X-LINKED MENTAL-RETARDATION
Authors: BILLUART P BIENVENU T RONCE N DESPORTES V VINET MC ZEMNI R CROLLIUS HR CARRIE A FAUCHEREAU F CHERRY M BRIAULT S HAMEL B FRYNS JP BELDJORD C KAHN A MORAINE C CHELLY J
Citation: P. Billuart et al., OLIGOPHRENIN-1 ENCODES A RHOGAP PROTEIN INVOLVED IN X-LINKED MENTAL-RETARDATION, Nature, 392(6679), 1998, pp. 923-926
MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W DEBOULLE K HENDRICKX J BAKKER E VANHOENACKER F MOLLICA F LUDECKE HJ SAYLI BS PAZZAGLIA UE MORTIER G HAMEL B CONRAD EU MATSUSHITA M RASKIND WH WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
MYCOBACTERIUM-AVIUM COMPLEX INFECTIONS - A REVIEW OF TREATMENTS
Authors: BRANDISSOU S HAMEL B VEILLET B KINOWSKI JM YAGOUBI N BRESSOLLE F
Citation: S. Brandissou et al., MYCOBACTERIUM-AVIUM COMPLEX INFECTIONS - A REVIEW OF TREATMENTS, Therapie, 52(1), 1997, pp. 65-71
RESTRUCTURING IN GLOBAL ALUMINUM - CAMPBE LL,B, ERICSSON,M
Authors: HAMEL B
Citation: B. Hamel, RESTRUCTURING IN GLOBAL ALUMINUM - CAMPBE LL,B, ERICSSON,M, Canadian journal of political science, 30(4), 1997, pp. 773-774
JENSEN-SYNDROME IS ALLELIC TO MOHR-TRANEBJAERG-SYNDROME AND BOTH ARE CAUSED BY STOP MUTATIONS IN THE DDP GENE
Authors: TRANEBJAERG L VANGHELUE M NILSSEN O HODES ME DLOUHY SR FARLOW MR HAMEL B ARTS WFM JANKOVIC J BEACH J JENSEN PKA
Citation: L. Tranebjaerg et al., JENSEN-SYNDROME IS ALLELIC TO MOHR-TRANEBJAERG-SYNDROME AND BOTH ARE CAUSED BY STOP MUTATIONS IN THE DDP GENE, American journal of human genetics, 61(4), 1997, pp. 2043-2043
GENETIC-MAPPING OF THE HUMAN HOMOLOG (T) OF MOUSE T(BRACHYURY) AND A SEARCH FOR ALLELE ASSOCIATION BETWEEN HUMAN T AND SPINA-BIFIDA
Authors: MORRISON K PAPAPETROU C ATTWOOD J HOL F LYNCH SA SAMPATH A HAMEL B BURN J SOWDEN J STOTT D MARIMAN E EDWARDS YH
Citation: K. Morrison et al., GENETIC-MAPPING OF THE HUMAN HOMOLOG (T) OF MOUSE T(BRACHYURY) AND A SEARCH FOR ALLELE ASSOCIATION BETWEEN HUMAN T AND SPINA-BIFIDA, Human molecular genetics, 5(5), 1996, pp. 669-674
UNTHINKING SOCIAL-SCIENCE - THE LIMITS OF 19TH-CENTURY PARADIGMS - FRENCH - WALLERSTEIN,I
Authors: HAMEL B
Citation: B. Hamel, UNTHINKING SOCIAL-SCIENCE - THE LIMITS OF 19TH-CENTURY PARADIGMS - FRENCH - WALLERSTEIN,I, Canadian journal of political science, 29(3), 1996, pp. 621-623
GOVERNMENT AND POLITICS IN THE UNITED-STA TES - FRENCH - BROWN,BE
Authors: HAMEL B
Citation: B. Hamel, GOVERNMENT AND POLITICS IN THE UNITED-STA TES - FRENCH - BROWN,BE, Canadian journal of political science, 28(3), 1995, pp. 578-579
NONSPECIFIC X-LINKED MENTAL-RETARDATION - IDENTIFICATION OF SEPARATE SUBTYPES BY LINKAGE STUDIES AND DETAILED CLINICAL INVESTIGATION
Authors: SMITS A MARIMAN E VANDENHELM B KNOERSVANSLOBBE N SMEETS D KREMER H VANDERMAAREL S HAMEL B ROPERS HH
Citation: A. Smits et al., NONSPECIFIC X-LINKED MENTAL-RETARDATION - IDENTIFICATION OF SEPARATE SUBTYPES BY LINKAGE STUDIES AND DETAILED CLINICAL INVESTIGATION, Cytogenetics and cell genetics, 67(4), 1994, pp. 350-350
INVESTIGATING THE INVOLVEMENT OF 18Q23 IN THE ETIOLOGY OF WILLIAMS-SYNDROME
Authors: SCHEPENS M NIEUWINT A VANDEVELDEVISSER S MERK G VANKESSEL AG OVERHAUSER J DONNAI D ARWERT F HAMEL B MENKO F MARIMAN E
Citation: M. Schepens et al., INVESTIGATING THE INVOLVEMENT OF 18Q23 IN THE ETIOLOGY OF WILLIAMS-SYNDROME, Cytogenetics and cell genetics, 65(3), 1994, pp. 162-162
CLINICAL AND MOLECULAR STUDIES IN A LARGE DUTCH FAMILY WITH NOONAN SYNDROME
Authors: VANDERBURGT I BERENDS E LOMMEN E VANBEERSUM S HAMEL B MARIMAN E
Citation: I. Vanderburgt et al., CLINICAL AND MOLECULAR STUDIES IN A LARGE DUTCH FAMILY WITH NOONAN SYNDROME, American journal of medical genetics, 53(2), 1994, pp. 187-191
PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH
Authors: SMITS A SMEETS D HAMEL B DREESEN J DEHAAN A VANOOST B
Citation: A. Smits et al., PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH, American journal of medical genetics, 51(4), 1994, pp. 497-500
THE GENE FOR SPONDYLOEPIPHYSEAL DYSPLASIA (SEDL) MAPS TO XP22 BETWEENDXS16 AND DXS92
Authors: HEUERTZ S NELEN M WILKIE AOM LEMERRER M DELRIEU O LARGETPIET L TRANEBJAERG L BICK D HAMEL B VANOOST BA MAROTEAUX P HORSCAYLA MC
Citation: S. Heuertz et al., THE GENE FOR SPONDYLOEPIPHYSEAL DYSPLASIA (SEDL) MAPS TO XP22 BETWEENDXS16 AND DXS92, Genomics, 18(1), 1993, pp. 100-104
MARDEN-WALKER SYNDROME - CASE-REPORT, LITERATURE-REVIEW AND NOSOLOGICDISCUSSION
Authors: SCHRANDERSTUMPEL C DEDIESMULDERS C DEKROM M SCHYNSFLEUREN S HAMEL B JAEKEN D FRYNS JP
Citation: C. Schranderstumpel et al., MARDEN-WALKER SYNDROME - CASE-REPORT, LITERATURE-REVIEW AND NOSOLOGICDISCUSSION, Clinical genetics, 43(6), 1993, pp. 303-308
TISSUE-SPECIFICITY STAGE-SPECIFICITY AND SPECIES-SPECIFICITY OF GENOMIC IMPRINTING IN MAN
Authors: KALSCHEUER V MARIMAN E SCHEPENS M HAMEL B REHDER H ROPERS HH
Citation: V. Kalscheuer et al., TISSUE-SPECIFICITY STAGE-SPECIFICITY AND SPECIES-SPECIFICITY OF GENOMIC IMPRINTING IN MAN, American journal of human genetics, 53(3), 1993, pp. 231-231
Risultati: 1-16 |