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Authors: MILLA E HEON E GROUNAUER PA PIGUET B DUCREY N STONE EM SCHORDERET DF MUNIER FL
Citation: E. Milla et al., RHODOPSIN C110Y MUTATION CAUSES A TYPE-2 AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA, Ophthalmic genetics, 19(3), 1998, pp. 131-139

Authors: MILLA E HEON E PIGUET B DUCREY N BUTLER N STONE E SCHORDERET DF MUNIER F
Citation: E. Milla et al., MUTATIONAL SCREENING OF PERIPHERINE RDS, RHODOPSINE AND ROM-1 GENES IN 69 INDEX PATIENTS WITH RETINITIS-PIGMENTOSA AND ALLIED RETINAL DYSTROPHIES/, Klinische Monatsblatter fur Augenheilkunde, 212(5), 1998, pp. 305-308

Authors: WONG AMF HEON E
Citation: Amf. Wong et E. Heon, HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION IN ABETALIPOPROTEINEMIA, Archives of ophthalmology, 116(2), 1998, pp. 250-251

Authors: ALWARD WLM SEMINA EV KALENAK JW HEON E SHETH BP STONE EM MURRAY JC
Citation: Wlm. Alward et al., AUTOSOMAL-DOMINANT IRIS HYPOPLASIA IS CAUSED BY A MUTATION IN THE RIEGER-SYNDROME (RIEG PITX2) GENE/, American journal of ophthalmology, 125(1), 1998, pp. 98-100

Authors: HEON E LIU S BILLINGSLEY G BERNASCONI O TSIFILDIS C SCHORDERET DF MUNIER FL
Citation: E. Heon et al., GENE LOCALIZATION FOR ACULEIFORM CATARACT, ON CHROMOSOME 2Q33-35, American journal of human genetics, 63(3), 1998, pp. 921-926

Authors: OH J HO LL ALAMELLO S AMATO D ARMSTRONG L BELLUCCI S CARAKUSHANSKY G ELLIS JP FONG CT GREEN JS HEON E LEGIUS E LEVIN AV NIEUWENHUIS HK PINCKERS A TAMURA N WHITEFORD ML YAMASAKI H SPRITZ RA
Citation: J. Oh et al., MUTATION ANALYSIS OF PATIENTS WITH HERMANSKY-PUDLAK-SYNDROME - A FRAMESHIFT HOT-SPOT IN THE HPS GENE AND APPARENT LOCUS HETEROGENEITY, American journal of human genetics, 62(3), 1998, pp. 593-598

Authors: MUNIER FL THONNEY F BALMER A UFFER S HEON E VANMELLE G RUTZ HP PESCIA G SCHORDERET DF
Citation: Fl. Munier et al., PROGNOSTIC FACTORS ASSOCIATED WITH LOSS OF HETEROZYGOSITY AT THE RB1 LOCUS IN RETINOBLASTOMA, Ophthalmic genetics, 18(1), 1997, pp. 7-12

Authors: HEON E MUNIER F TSIFILDIS C LIU S
Citation: E. Heon et al., MAPPING OF CONGENITAL ACULEIFORM CATARACT TO CHROMOSOME 2Q33, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4348-4348

Authors: MUNIER F KORVATSKA E DJEMAI A WANG MX HEON E CHIOU A UFFER S OTHENINGIRARD P HIROZ A BALESTRAZZI E FORSTER RK CULBERTSON WW ZOGRAFOS L SCHORDERET DF
Citation: F. Munier et al., 5Q31-LINKED CORNEAL DYSTROPHIES - GENOTYPE-PHENOTYPE CORRELATION AT THE KERATO-EPITHELIN GENE LOCUS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4454-4454

Authors: CONTRACTOR M MACKEEN L GALLIE BL MUNIER F PAVLIN CJ HAHN K LU Y HEON E UFFER S
Citation: M. Contractor et al., VISUALIZATION OF ANTERIOR EXTENT OF RETINOBLASTOMA USING ULTRASOUND BIOMICROSCOPY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 5216-5216

Authors: KOVACS R LEVIN AV DASILVA L MULLER W HEON E TSILFIDIS C
Citation: R. Kovacs et al., AUTOSOMAL-DOMINANT CONGENITAL CATARACTS WITH A POSTERIOR SUBCAPSULAR PHENOTYPE SHOW POTENTIAL LINKAGE TO THE ALPHA-A-CRYSTALLIN ON CHROMOSOME-21, Investigative ophthalmology & visual science, 38(4), 1997, pp. 2719-2719

Authors: LIU S CHEUNG JC HEON E
Citation: S. Liu et al., THE GENETICS OF GLAUCOMA - AN UPDATE, Canadian journal of ophthalmology, 32(4), 1997, pp. 221-228

Authors: BILLINGSLEY GD MUNIER F LIU S TSIFILDIS C HEON E
Citation: Gd. Billingsley et al., REFINED LOCALIZATION OF THE CONGENITAL ACULEIFORM CATARACT, American journal of human genetics, 61(4), 1997, pp. 1562-1562

Authors: PIGUET B HEON E MUNIER FL GROUNAUER PA NIEMEYER G BUTLER N SCHORDERET DF SHEFFIELD VC STONE EM
Citation: B. Piguet et al., FULL CHARACTERIZATION OF THE MACULOPATHY ASSOCIATED WITH AN ARG-172-TRP MUTATION IN THE RDS PERIPHERIN GENE/, Ophthalmic genetics, 17(4), 1996, pp. 175-186

Authors: MUNIER F BALMER A HEON E UFFER S DEGOTTRAU P ZOGRAFOS L
Citation: F. Munier et al., PHENOTYPIC VARIABILITY AND REACTIVATION PATTERNS OF RETINOMA, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2875-2875

Authors: TSILFIDIS C LEVIN AV MULLER W DASILVA L HEON E
Citation: C. Tsilfidis et al., GENETIC-ANALYSIS OF AUTOSOMAL-DOMINANT CONGENITAL CATARACTS, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4540-4540

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

Authors: MUNIER F BALMER A LIU S TSIFILDIS C HEON E
Citation: F. Munier et al., STUDY OF CRYSTALLINE GENES IN AN AUTOSOMAL RECESSIVE CATARACT PHENOTYPE, Vision research, 36, 1996, pp. 3131-3131

Authors: MUNIER FL THONNEY F BALMER A HEON E PESCIA G SCHORDERET DF
Citation: Fl. Munier et al., SEX MUTATION RATIO IN RETINOBLASTOMA AND RETINOMA - RELEVANCE TO GENETIC-COUNSELING, Klinische Monatsblatter fur Augenheilkunde, 208(5), 1996, pp. 400-403

Authors: MICHAUD JL HEON E GUILBERT F WEILL J PUECH B BENSON L SMALLHORN JF SHUMAN CT BUNCIC JR LEVIN AV WEKSBERG R BREVIERE GM
Citation: Jl. Michaud et al., NATURAL-HISTORY OF ALSTROM-SYNDROME IN EARLY-CHILDHOOD - ONSET WITH DILATED CARDIOMYOPATHY, The Journal of pediatrics, 128(2), 1996, pp. 225-229

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

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

Authors: HEON E MATHERS WD ALWARD WLM WEISENTHAL RW SUNDEN SLF FISHBAUGH JA TAYLOR CM KRACHMER JH SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY TO 20Q11, Human molecular genetics, 4(3), 1995, pp. 485-488

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

Authors: HEON E MATHERS WD ALWARD WLM WEISENTHAL RW SUNDEN SLF FISHBAUGH J TAYLOR CM KRACHMER JH SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE ANALYSIS OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY AND ASSESSMENT OF GENETIC-HETEROGENEITY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 771-771
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