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Results: 1-8 |
Results: 8

Authors: HUXLEY C PASSAGE E ROBERTSON AM YOUL B HUSTON S MANSON A SABERANDJONIEDI D FIGARELLABRANGER D PELLISSIER JF THOMAS PK FONTES M
Citation: C. Huxley et al., CORRELATION BETWEEN VARYING LEVELS OF PMP22 EXPRESSION AND THE DEGREEOF DEMYELINATION AND REDUCTION IN NERVE-CONDUCTION VELOCITY IN TRANSGENIC MICE, Human molecular genetics, 7(3), 1998, pp. 449-458

Authors: HUGNOT JP PEDEUTOUR F LECALVEZ C GROSGEORGE J PASSAGE E FONTES M LAZDUNSKI M
Citation: Jp. Hugnot et al., THE HUMAN INWARD RECTIFYING K-2.2 (KCNJ12) GENE - GENE STRUCTURE, ASSIGNMENT TO CHROMOSOME 17P11.1, AND IDENTIFICATION OF A SIMPLE TANDEM REPEAT POLYMORPHISM( CHANNEL KIR), Genomics, 39(1), 1997, pp. 113-116

Authors: HUXLEY C PASSAGE E MANSON A PUTZU G FIGARELLABRANGER D PELLISSIER JF FONTES M
Citation: C. Huxley et al., CONSTRUCTION OF A MOUSE MODEL OF CHARCOT-MARIE-TOOTH DISEASE TYPE 1A BY PRONUCLEAR INJECTION OF HUMAN YAC DNA, Human molecular genetics, 5(5), 1996, pp. 563-569

Authors: VILLARD L PASSAGE E COLLEAUX L FONTES M
Citation: L. Villard et al., USE OF INTERSPERSED REPETITIVE SEQUENCES-PCR PRODUCTS FOR CDNA SELECTION, Mammalian genome, 6(9), 1995, pp. 617-622

Authors: GECZ J GAUNT SJ PASSAGE E BURTON RD CUDREY C PEARCE JJH FONTES M
Citation: J. Gecz et al., ASSIGNMENT OF A POLYCOMB-LIKE CHROMOBOX GENE (CBX2) TO HUMAN-CHROMOSOME 17Q25, Genomics, 26(1), 1995, pp. 130-133

Authors: CUDREY C CHEVILLARD C LEPASLIER D VIGNAL A PASSAGE E FONTES M
Citation: C. Cudrey et al., ASSIGNMENT OF MICROSATELLITE SEQUENCES TO THE REGION DUPLICATED IN CMT1A (17P12) - A USEFUL TOOL FOR DIAGNOSIS, Journal of Medical Genetics, 32(3), 1995, pp. 231-233

Authors: LIBERT F PASSAGE E PARMENTIER M SIMONS MJ VASSART G MATTEI MG
Citation: F. Libert et al., CHROMOSOMAL MAPPING OF A1-ADENOSINE AND A2-ADENOSINE RECEPTORS, VIP RECEPTOR, AND A NEW SUBTYPE OF SEROTONIN RECEPTOR (VOL 11, PG 225, 1991), Genomics, 23(1), 1994, pp. 305-305

Authors: CHEVILLARD C LEPASLIER D PASSAGE E OUGEN P BILLAULT A BOYER S MAZAN S BACHELLERIE JP VIGNAL A COHEN D FONTES M
Citation: C. Chevillard et al., RELATIONSHIP BETWEEN CHARCOT-MARIE-TOOTH-1A AND SMITH-MAGENIS REGIONS- SNU3 MAY BE A CANDIDATE GENE FOR THE SMITH-MAGENIS SYNDROME, Human molecular genetics, 2(8), 1993, pp. 1235-1243
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