AAAAAA

   
Results: 1-22 |
Results: 22
EVALUATION OF A SIGNIFICANTLY SHORTER VERSION OF THE FARNSWORTH-MUNSELL 100-HUE TEST IN PATIENTS WITH 3 DIFFERENT OPTIC NEUROPATHIES
Authors: NICHOLS BE THOMPSON HS STONE EM
Citation: Be. Nichols et al., EVALUATION OF A SIGNIFICANTLY SHORTER VERSION OF THE FARNSWORTH-MUNSELL 100-HUE TEST IN PATIENTS WITH 3 DIFFERENT OPTIC NEUROPATHIES, Journal of neuro-ophthalmology, 17(1), 1997, pp. 1-6
IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA
Authors: FINGERT JH ALWARD WLM SUNDEN SLF NISHIMURA D NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER BECK GE STREB LM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4333-4333
CLINICAL CHARACTERIZATION AND LINKAGE ANALYSIS OF A 4 GENERATION FAMILY WITH CONE-ROD DYSTROPHY
Authors: BROWN J NICHOLS BE WILES CD BUTLER N SHEFFIELD VC STONE EM
Citation: J. Brown et al., CLINICAL CHARACTERIZATION AND LINKAGE ANALYSIS OF A 4 GENERATION FAMILY WITH CONE-ROD DYSTROPHY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 5339-5339
IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA
Authors: STONE EM FINGERT JH ALWARD WLM NGUYEN TD POLANSKY JR SUNDEN SLF NISHIMURA D CLARK AF NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER SHEFFIELD VC
Citation: Em. Stone et al., IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA, Science, 275(5300), 1997, pp. 668-670
FINE MAPPING OF THE AUTOSOMAL-DOMINANT JUVENILE OPEN-ANGLE GLAUCOMA (GLCLA) REGION AND EVALUATION OF CANDIDATE GENES
Authors: SUNDEN SLF ALWARD WLM NICHOLS BE ROKHLINA TR NYSTUEN A STONE EM SHEFFIELD VC
Citation: Slf. Sunden et al., FINE MAPPING OF THE AUTOSOMAL-DOMINANT JUVENILE OPEN-ANGLE GLAUCOMA (GLCLA) REGION AND EVALUATION OF CANDIDATE GENES, PCR methods and applications, 6(9), 1996, pp. 862-869
HIGH-DENSITY MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMA REGION
Authors: SHEFFIELD VC SUNDEN SLF ALWARD WLM ROHKLINA RT NICHOLS BE STONE EM
Citation: Vc. Sheffield et al., HIGH-DENSITY MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMA REGION, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2078-2078
PHYSICAL AND GENETIC FINE MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMAREGION (1Q21-Q31)
Authors: SUNDEN SLF NICHOLS BE ALWARD WLM NISHIMURA DY STONE EM SHEFFIELD VC
Citation: Slf. Sunden et al., PHYSICAL AND GENETIC FINE MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMAREGION (1Q21-Q31), American journal of human genetics, 57(4), 1995, pp. 1174-1174
3 AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES MAP TO CHROMOSOME-5Q
Authors: STONE EM MATHERS WD ROSENWASSER GOD HOLLAND EJ FOLBERG R KRACHMER JH NICHOLS BE GOREVIC PD TAYLOR CM STREB LM FISHBAUGH JA DALEY TE SUCHESKI BM SHEFFIELD VC
Citation: Em. Stone et al., 3 AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES MAP TO CHROMOSOME-5Q, Nature genetics, 6(1), 1994, pp. 47-51
FINE MAPPING OF THE PRIMARY OPEN-ANGLE GLAUCOMA LOCUS ON CHROMOSOME-1
Authors: NICHOLS BE ALWARD WLM RITCH R STREB LM TAYLOR CM SUNDEN SLF SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., FINE MAPPING OF THE PRIMARY OPEN-ANGLE GLAUCOMA LOCUS ON CHROMOSOME-1, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1470-1470
INCIDENCE OF FRAMESHIFT MUTATIONS IN THE PROCOLLAGEN II GENE IN STICKLER SYNDROME AND IDENTIFICATION OF 4 NEW MUTATIONS
Authors: BROWN DM VANDENBURGH K NICHOLS BE KIMURA AE WEINGEIST TA SHEFFIELD VC STONE EM
Citation: Dm. Brown et al., INCIDENCE OF FRAMESHIFT MUTATIONS IN THE PROCOLLAGEN II GENE IN STICKLER SYNDROME AND IDENTIFICATION OF 4 NEW MUTATIONS, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1717-1717
GENETIC-LINKAGE OF A STARGARDT-LIKE DOMINANT PROGRESSIVE MACULAR DYSTROPHY TO CHROMOSOME-6
Authors: STONE EM NICHOLS BE KIMURA AE WEINGEIST TA DRACK AV SHEFFIELD VC
Citation: Em. Stone et al., GENETIC-LINKAGE OF A STARGARDT-LIKE DOMINANT PROGRESSIVE MACULAR DYSTROPHY TO CHROMOSOME-6, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1717-1717
CLINICAL-FEATURES OF A STARGARDT-LIKE DOMINANT PROGRESSIVE MACULAR DYSTROPHY WITH GENETIC-LINKAGE TO CHROMOSOME 6Q
Authors: STONE EM NICHOLS BE KIMURA AE WEINGEIST TA DRACK A SHEFFIELD VC
Citation: Em. Stone et al., CLINICAL-FEATURES OF A STARGARDT-LIKE DOMINANT PROGRESSIVE MACULAR DYSTROPHY WITH GENETIC-LINKAGE TO CHROMOSOME 6Q, Archives of ophthalmology, 112(6), 1994, pp. 765-772
REFINING THE LOCUS FOR BEST VITELLIFORM MACULAR DYSTROPHY AND MUTATION ANALYSIS OF THE CANDIDATE GENE ROM-I
Authors: NICHOLS BE BASCOM R LITT M MCINNES R SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., REFINING THE LOCUS FOR BEST VITELLIFORM MACULAR DYSTROPHY AND MUTATION ANALYSIS OF THE CANDIDATE GENE ROM-I, American journal of human genetics, 54(1), 1994, pp. 95-103
GENETIC-LINKAGE OF FAMILIAL OPEN-ANGLE GLAUCOMA TO CHROMOSOME-1Q21-Q31
Authors: SHEFFIELD VC STONE EM ALWARD WLM DRACK AV JOHNSON AT STREB LM NICHOLS BE
Citation: Vc. Sheffield et al., GENETIC-LINKAGE OF FAMILIAL OPEN-ANGLE GLAUCOMA TO CHROMOSOME-1Q21-Q31, Nature genetics, 4(1), 1993, pp. 47-50
A 2-BASE PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA (VOL 2, PG 601, 1993)
Authors: NICHOLS BE DRACK AV VANDENBURGH K KIMURA AE SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., A 2-BASE PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA (VOL 2, PG 601, 1993), Human molecular genetics, 2(8), 1993, pp. 1347-1347
A 2 BASE-PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA
Authors: NICHOLS BE DRACK AV VANDENBURGH K KIMURA AE SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., A 2 BASE-PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA, Human molecular genetics, 2(5), 1993, pp. 601-603
A USER-FRIENDLY HYPERCARD INTERFACE FOR HUMAN LINKAGE ANALYSIS
Authors: NICHOLS BE SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., A USER-FRIENDLY HYPERCARD INTERFACE FOR HUMAN LINKAGE ANALYSIS, Computer applications in the biosciences, 9(6), 1993, pp. 757-759
MUTATIONS IN THE RDS PERIPHERIN GENE CAUSE WIDELY DIFFERENT PHENOTYPES BETWEEN AND WITHIN AFFECTED FAMILIES
Authors: STONE EM NICHOLS BE KIMURA AE WELEBER RG GORIN MB FISHMAN GA JACOBSON SG GASS JDM DRACK AV VANDENBURGH K SHEFFIELD VC
Citation: Em. Stone et al., MUTATIONS IN THE RDS PERIPHERIN GENE CAUSE WIDELY DIFFERENT PHENOTYPES BETWEEN AND WITHIN AFFECTED FAMILIES, American journal of human genetics, 53(3), 1993, pp. 14-14
FINE MAPPING OF THE BESTS-DISEASE LOCUS AND MUTATION ANALYSIS OF THE CANDIDATE GENE ROM1
Authors: NICHOLS BE BASCOM RA LITT M MCINNES R TAYLOR CM SHEFFIELD VC STONE EM
Citation: Be. Nichols et al., FINE MAPPING OF THE BESTS-DISEASE LOCUS AND MUTATION ANALYSIS OF THE CANDIDATE GENE ROM1, American journal of human genetics, 53(3), 1993, pp. 1050-1050
GENETIC-MAPPING OF FAMILIAL OPEN-ANGLE GLAUCOMA TO CHROMOSOME 1Q21-Q31 AND ANALYSIS OF CANDIDATE GENES
Authors: SHEFFIELD VC NICHOLS BE ALWARD WLM DRACK AV JOHNSON AT STREB LM STONE EM
Citation: Vc. Sheffield et al., GENETIC-MAPPING OF FAMILIAL OPEN-ANGLE GLAUCOMA TO CHROMOSOME 1Q21-Q31 AND ANALYSIS OF CANDIDATE GENES, American journal of human genetics, 53(3), 1993, pp. 1075-1075
GENETIC MUTATIONS AT THE C-TERMINAL END OF THE PROCOLLAGEN-II GENE INSTICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY) AND IDENTIFICATION AND PHENOTYPIC DESCRIPTION OF A NEW MUTATION
Authors: BROWN DM VANDENBURGH K NICHOLS BE ERHART AR KIMURA AE WEINGEIST TA SHEFFIELD VC STONE EM
Citation: Dm. Brown et al., GENETIC MUTATIONS AT THE C-TERMINAL END OF THE PROCOLLAGEN-II GENE INSTICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY) AND IDENTIFICATION AND PHENOTYPIC DESCRIPTION OF A NEW MUTATION, American journal of human genetics, 53(3), 1993, pp. 1133-1133
IDENTIFICATION OF MITOCHONDRIAL GENE-MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC NEUROPATHY BY GC-CLAMPED DENATURING GRADIENT GEL-ELECTROPHORESIS
Authors: COPPINGER JM NICHOLS BE STREB LM MACK RI SHEFFIELD VC STONE EM
Citation: Jm. Coppinger et al., IDENTIFICATION OF MITOCHONDRIAL GENE-MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC NEUROPATHY BY GC-CLAMPED DENATURING GRADIENT GEL-ELECTROPHORESIS, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1221-1221
Risultati: 1-22 |