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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
Citation: Amf. Wong et E. Heon, HELICOID PERIPAPILLARY CHORIORETINAL DEGENERATION IN ABETALIPOPROTEINEMIA, Archives of ophthalmology, 116(2), 1998, pp. 250-251
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ALWARD WLM
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KALENAK JW
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Authors:
HEON E
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BILLINGSLEY G
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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
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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
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Citation: E. Heon et al., MAPPING OF CONGENITAL ACULEIFORM CATARACT TO CHROMOSOME 2Q33, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4348-4348
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DJEMAI A
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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
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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
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MUNIER F
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Citation: Gd. Billingsley et al., REFINED LOCALIZATION OF THE CONGENITAL ACULEIFORM CATARACT, American journal of human genetics, 61(4), 1997, pp. 1562-1562
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PIGUET B
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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
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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
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MUNIER FL
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PESCIA G
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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
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HEON E
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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
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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
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TAYLOR CM
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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
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HEON E
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ALWARD WLM
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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
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HEON E
MATHERS WD
ALWARD WLM
WEISENTHAL RW
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FISHBAUGH J
TAYLOR CM
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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