AAAAAA

   
Results: 1-13 |
Results: 13

Authors: LOYER M PESCHLOW A ROBITAILLE J TRABOULSI E LITTLE J POLOMENO R MAUMENEE I KAPLAN J KOENEKOOP R
Citation: M. Loyer et al., MUTATIONS IN THE GENE FOR RETINAL GUANYLATE-CYCLASE IN PATIENTS WITH LEBERS CONGENITAL AMAUROSIS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3180-3180

Authors: PESCHLOW A LOYER M WRAY M BENOIT J GOMOLIN J POLOMENO R LACHAPELLE P KOENEKOOP R
Citation: A. Peschlow et al., GENOTYPE-PHENOTYPE CORRELATIONS IN RP - DISPARATE ERG PHENOTYPES IN NONSENSE AND MISSENSE RHODOPSIN MUTATIONS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3710-3710

Authors: COTE G LESAGE A CHAWKY N LOYER M
Citation: G. Cote et al., CLINICAL SPECIFICITY OF PRISON-INMATES WITH SEVERE MENTAL-DISORDERS -A CASE-CONTROL STUDY, British Journal of Psychiatry, 170, 1997, pp. 571-577

Authors: AKERMAN BR NATOWICZ MR KABACK MM LOYER M CAMPEAU E GRAVEL RA
Citation: Br. Akerman et al., NOVEL MUTATIONS AND DNA-BASED SCREENING IN NON-JEWISH CARRIERS OF TAY-SACHS-DISEASE, American journal of human genetics, 60(5), 1997, pp. 1099-1106

Authors: DAVIDSON JK TINK J LOYER M TRABOULSI E MAUMENEE I KOENEKOOP RK
Citation: Jk. Davidson et al., PIGMENT-EPITHELIUM DERIVED FACTOR AS A CANDIDATE GENE FOR LEBERS CONGENITAL AMAUROSIS, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4548-4548

Authors: LOYER M WISE L TRABOULSI E MAUMENEE I KOENEKOOP RK
Citation: M. Loyer et al., EVALUATION OF THE GENE ENCODING THE ALPHA-SUBUNIT OF CONE TRANSDUCIN IN LEBERS CONGENITAL AMAUROSIS AND OTHER RETINAL DYSTROPHIES, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4555-4555

Authors: WRAY M NARAYANAN P LACHAPELLE P LOYER M LITTLE JK POLOMENO B KOENEKOOP R
Citation: M. Wray et al., MOLECULAR AND ELECTROPHYSIOLOGICAL CORRELATIONS IN SYBTYPES OF RETINITIS-PIGMENTOSA, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4581-4581

Authors: WEIN F LOYER M GANS M MCMILLAN C KOENEKOOP R
Citation: F. Wein et al., A CLINICAL AND MOLECULAR ANALYSIS OF A QUEBEC PEDIGREE WITH LEBERS HEREDITARY OPTIC NEUROPATHY, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4586-4586

Authors: LOYER M LECLERC D GRAVEL RA
Citation: M. Loyer et al., INTERALLELIC COMPLEMENTATION OF BETA-SUBUNIT DEFECTS IN FIBROBLASTS OF PATIENTS WITH PROPIONYL-COA CARBOXYLASE DEFICIENCY MICROINJECTED WITH MUTANT CDNA CONSTRUCTS, Human molecular genetics, 4(6), 1995, pp. 1035-1039

Authors: LOYER M
Citation: M. Loyer, GERMAN INTELLIGENCE, 1939 40, Historia, (585), 1995, pp. 4-4

Authors: LAMHONWAH AM LECLERC D LOYER M CLARIZIO R GRAVEL RA
Citation: Am. Lamhonwah et al., CORRECTION OF THE METABOLIC DEFECT IN PROPIONIC ACIDEMIA FIBROBLASTS BY MICROINJECTION OF A FULL-LENGTH CDNA OR RNA TRANSCRIPT ENCODING THEPROPIONYL-COA CARBOXYLASE BETA-SUBUNIT, Genomics, 19(3), 1994, pp. 500-505

Authors: LESAGE AD BOYER R GRUNBERG F VANIER C MORISSETTE R MENARDBUTEAU C LOYER M
Citation: Ad. Lesage et al., SUICIDE AND MENTAL-DISORDERS - A CASE-CONTROL STUDY OF YOUNG MEN, The American journal of psychiatry, 151(7), 1994, pp. 1063-1068

Authors: GRAVEL RA AKERMAN BR LAMHONWAH AM LOYER M LEONDELRIO A ITALIANO I
Citation: Ra. Gravel et al., MUTATIONS PARTICIPATING IN INTERALLELIC COMPLEMENTATION IN PROPIONIC ACIDEMIA, American journal of human genetics, 55(1), 1994, pp. 51-58
Risultati: 1-13 |