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Results: 1-14 |
Results: 14
ALLELIC VARIATION IN ABCR ASSOCIATED WITH STARGARDT-DISEASE BUT NOT AGE-RELATED MACULAR DEGENERATION
Authors: STONE EM WEBSTER AR VANDENBURGH K STREB LM HOCKEY RR LOTERY AJ SHEFFIELD VC
Citation: Em. Stone et al., ALLELIC VARIATION IN ABCR ASSOCIATED WITH STARGARDT-DISEASE BUT NOT AGE-RELATED MACULAR DEGENERATION, Nature genetics, 20(4), 1998, pp. 328-329
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 AND HAPLOTYPIC CHARACTERIZATION OF 14 FAMILIES AFFECTED WITHRADIAL DRUSEN (MALATTIA-LEVENTINESE)
Authors: HEON E PIGUET B MUNIER FL SNEED SR MORGAN C FORNI S SCHORDERET D POLK TD TAYLOR CM STREB LM WILES CD SHEFFIELD VC STONE EM
Citation: E. Heon et al., CLINICAL AND HAPLOTYPIC CHARACTERIZATION OF 14 FAMILIES AFFECTED WITHRADIAL DRUSEN (MALATTIA-LEVENTINESE), Investigative ophthalmology & visual science, 37(3), 1996, pp. 5163-5163
LINKAGE OF AUTOSOMAL-DOMINANT RADIAL DRUSEN (MALATTIA LEVENTINESE) TOCHROMOSOME 2P16-21
Authors: HEON E PIGUET B MUNIER F SNEED SR MORGAN CM FORNI S PESCIA G SCHORDERET D TAYLOR CM STREB LM WILES CD NISHIMURA DY SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT RADIAL DRUSEN (MALATTIA LEVENTINESE) TOCHROMOSOME 2P16-21, Archives of ophthalmology, 114(2), 1996, pp. 193-198
LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25)
Authors: HEON E SHETH BP KALENAK JW SUNDEN SLF STREB LM TAYLOR CM ALWARD WLM SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25), Human molecular genetics, 4(8), 1995, pp. 1435-1439
CLINICAL AND MOLECULAR EVALUATION OF A LARGE FAMILY WITH IRIS HYPOPLASIA AND GLAUCOMA
Authors: SHETH B HEON E KALENAK J TAYLOR CM STREB LM ALWARD WLM STONE EM SHEFFIELD VC
Citation: B. Sheth et al., CLINICAL AND MOLECULAR EVALUATION OF A LARGE FAMILY WITH IRIS HYPOPLASIA AND GLAUCOMA, Investigative ophthalmology & visual science, 36(4), 1995, pp. 554-554
LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE RIEGER SYNDROME LOCUS (4Q25)
Authors: HEON E SHETH BP KALENAK JW SUNDEN SLF STREB LM TAYLOR CM MUNDEN P ALWARD WLM SHEFFIELD VL STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE RIEGER SYNDROME LOCUS (4Q25), Vision research, 35, 1995, pp. 3127-3127
GENETIC-LINKAGE OF WAGNER DISEASE AND EROSIVE VITREORETINOPATHY TO CHROMOSOME 5Q13-14
Authors: BROWN DM GRAEMIGER RA HERGERSBERG M SCHINZEL A MESSMER EP NIEMEYER G SCHNEEBERGER SA STREB LM TAYLOR CM KIMURA AE WEINGEIST TA SHEFFIELD C STONE EM
Citation: Dm. Brown et al., GENETIC-LINKAGE OF WAGNER DISEASE AND EROSIVE VITREORETINOPATHY TO CHROMOSOME 5Q13-14, Archives of ophthalmology, 113(5), 1995, pp. 671-675
LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE RIEGER SYNDROME LOCUS (4Q25)
Authors: HEON E SHETH BP KALENAK JW SUNDEN SLF STREB LM TAYLOR CM MUNDEN P ALWARD WLM SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE RIEGER SYNDROME LOCUS (4Q25), American journal of human genetics, 57(4), 1995, pp. 1108-1108
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
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
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
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
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