AAAAAA

   
Results: 1-13 |
Results: 13

Authors: LEVY G LEVIACOBAS F BLANCHARD S GERBER S LARGETPIET D CHENAL V LIU XZ NEWTON V STEEL KP BROWN SDM MUNNICH A KAPLAN J PETIT C WEIL D
Citation: G. Levy et al., MYOSIN VIIA GENE - HETEROGENEITY OF THE MUTATIONS RESPONSIBLE FOR USHER-SYNDROME TYPE IB, Human molecular genetics, 6(1), 1997, pp. 111-116

Authors: GERBER S LARGETPIET D ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: S. Gerber et al., EVIDENCE FOR A FOURTH LOCUS IN USHER SYNDROME TYPE-I, Journal of Medical Genetics, 33(1), 1996, pp. 77-79

Authors: KAPLAN J ROZET JM GERBER S CAMUZAT A SOUIED E BONNEAU D LARGETPIET D DOLLFUS H DUFIER JL BRIARD ML FREZAL J MUNNICH A
Citation: J. Kaplan et al., GENES FOR CHILDHOOD RETINAL DYSTROPHIES, MS. Medecine sciences, 11(3), 1995, pp. 325-335

Authors: LARGETPIET D GERBER S ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER SYNDROME TYPE-I (USID), Vision research, 35, 1995, pp. 3234-3234

Authors: WELL D BLANCHARD S KAPLAN J GUILFORD P GIBSON F WALSH J MBURU P VARELA A LEVILLERS J WESTON MD KELLEY PM KIMBERLING WJ WAGENAAR M LEVIACOBAS F LARGETPIET D MUNNICH A STEEL KP BROWN SDM PETIT C
Citation: D. Well et al., DEFECTIVE MYOSIN VIIA GENE RESPONSIBLE FOR USHER SYNDROME TYPE 1B, Nature, 374(6517), 1995, pp. 60-61

Authors: LARGETPIET D GERBER S ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER-SYNDROME TYPE-I (USID), American journal of human genetics, 57(4), 1995, pp. 1885-1885

Authors: KAPLAN J GERBER S LARGETPIET D ROZET JM DOLLFUS H DUFIER JL ODENT S POSTELVINAY A JANIN N BRIARD ML FREZAL J MUNNICH A
Citation: J. Kaplan et al., A GENE FOR STARGARDTS-DISEASE (FUNDUS-FLAVIMACULATUS) MAPS TO THE SHORT ARM OF CHROMOSOME-1, Nature genetics, 6(2), 1994, pp. 214-214

Authors: LARGETPIET D GERBER S BONNEAU D ROZET JM MARC S GHAZI I DUFIER JL DAVID A BITOUN P WEISSENBACH J MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., GENETIC-HETEROGENEITY OF USHER SYNDROME TYPE-1 IN FRENCH FAMILIES, Genomics, 21(1), 1994, pp. 138-143

Authors: DINGEON B DUBIN F FARRIAUX JP LARGETPIET D LEMAY C DESMET G MOINEAU MP MORIN JF POLOCE F RUFFIE A THIBAUD D VALAT C BESNARD JC
Citation: B. Dingeon et al., SCREENING OF FETUSES WITH RISK OF TRISOMY -21, La Presse medicale, 23(11), 1994, pp. 505-506

Authors: KAPLAN J LARGETPIET D GERBER S BONNEAU D DOLLFUS H ROZET JM MUNNICH A
Citation: J. Kaplan et al., REFINING OF THE GENETIC-MAPPING OF US1A (14Q32), Cytogenetics and cell genetics, 66(1), 1994, pp. 13-13

Authors: KAPLAN J GERBER S LARGETPIET D ROZET JM DOLLFUS H DUFIER JL ODENT S POSTELVINAY A JANIN N BRIARD ML FREZAL J MUNNICH A
Citation: J. Kaplan et al., A GENE FOR STARGARDTS-DISEASE (FUNDUS-FLAVIMACULATUS) MAPS TO THE SHORT ARM OF CHROMOSOME-1, Nature genetics, 5(3), 1993, pp. 308-311

Authors: LARGETPIET D ROZET JM GERBER S DOLLFUS H MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN PROTEIN-C INHIBITOR (PCI) LOCUS, Human molecular genetics, 2(12), 1993, pp. 2201-2201

Authors: COZON G ROURE C LIZARD G GREENLAND T LARGETPIET D GANDILHON F PEYRON F
Citation: G. Cozon et al., AN IMPROVED ASSAY FOR THE DETECTION OF TOXOPLASMA-GONDII ANTIBODIES IN HUMAN SERUM BY FLOW-CYTOMETRY, Cytometry, 14(5), 1993, pp. 569-575
Risultati: 1-13 |