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Results: 1-25 | 26-26
Results: 1-25/26
DRES93, A NOVEL HOMEODOMAIN-CONTAINING CDNA SELECTIVELY EXPRESSED IN THE DEVELOPING RETINA IS A CANDIDATE FOR HUMAN EYE MALFORMATIONS
Authors: BARBIERI AM BULFONE A MARCHITIELLO A MUNIER F BITOUN P SCHORDERET DF BORSANI G BALLABIO A BANFI S
Citation: Am. Barbieri et al., DRES93, A NOVEL HOMEODOMAIN-CONTAINING CDNA SELECTIVELY EXPRESSED IN THE DEVELOPING RETINA IS A CANDIDATE FOR HUMAN EYE MALFORMATIONS, European journal of human genetics, 6, 1998, pp. 4132-4132
USE OF SPERM-TYPING TECHNIQUE TO ACCURATELY DETERMINE THE RECOMBINATION FREQUENCY BETWEEN THE RB1 GENE AND AN EXTRAGENIC POLYMORPHISM
Authors: GIRARDET A LEEFLANG E LIEN S ARNHEIM N MUNIER F CLAUSTRES M PELLESTOR F
Citation: A. Girardet et al., USE OF SPERM-TYPING TECHNIQUE TO ACCURATELY DETERMINE THE RECOMBINATION FREQUENCY BETWEEN THE RB1 GENE AND AN EXTRAGENIC POLYMORPHISM, European journal of human genetics, 6, 1998, pp. 4197-4197
IMAGING IN CHILDREN WITH INTRAOCULAR LESI ONS
Authors: BALMER A MUNIER F UFFER S
Citation: A. Balmer et al., IMAGING IN CHILDREN WITH INTRAOCULAR LESI ONS, Klinische Monatsblatter fur Augenheilkunde, 212(5), 1998, pp. 252-256
MUTATIONAL SCREENING OF PERIPHERINE RDS, RHODOPSINE AND ROM-1 GENES IN 69 INDEX PATIENTS WITH RETINITIS-PIGMENTOSA AND ALLIED RETINAL DYSTROPHIES/
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
AMPLIFICATION OF THE RB1.20 POLYMORPHISM IN SINGLE SPERMATOZOA
Authors: GIRARDET A PELLESTOR F TUFFERY S CLAUSTRES M MUNIER F DUPERRAY C
Citation: A. Girardet et al., AMPLIFICATION OF THE RB1.20 POLYMORPHISM IN SINGLE SPERMATOZOA, Journal of assisted reproduction and genetics, 14(3), 1997, pp. 176-179
MAPPING OF CONGENITAL ACULEIFORM CATARACT TO CHROMOSOME 2Q33
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
5Q31-LINKED CORNEAL DYSTROPHIES - GENOTYPE-PHENOTYPE CORRELATION AT THE KERATO-EPITHELIN GENE LOCUS
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
VISUALIZATION OF ANTERIOR EXTENT OF RETINOBLASTOMA USING ULTRASOUND BIOMICROSCOPY
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
IDENTIFICATION OF NOVEL PAX6 MUTATIONS IN FAMILIAL ANIRIDIA
Authors: NEUNERJEHLE M MUNIER F SAHLY I SCHORDERET D MERMONT A UTEZA Y KOBETZ A MARCHANT D BECQUET F ABITBOL M DUFIER JL
Citation: M. Neunerjehle et al., IDENTIFICATION OF NOVEL PAX6 MUTATIONS IN FAMILIAL ANIRIDIA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 111-111
RHYZOMELIC CHONDRODYSPLASIA PUNCTATA ASSOCIATED WITH RETINITIS-PIGMENTOSA
Authors: SANCHEZ E MUNIER F NIEMEYER G GROUNAUER PA BALMER A
Citation: E. Sanchez et al., RHYZOMELIC CHONDRODYSPLASIA PUNCTATA ASSOCIATED WITH RETINITIS-PIGMENTOSA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1442-1442
OCULAR PHENOTYPE IN A CHILD WITH A RHIZOM ELIC CHONDRODYSPLASIA PUNCTATA
Authors: SANCHEZ E MUNIER F EVEQUOZ B MARCOZ JP BALMER A
Citation: E. Sanchez et al., OCULAR PHENOTYPE IN A CHILD WITH A RHIZOM ELIC CHONDRODYSPLASIA PUNCTATA, Klinische Monatsblatter fur Augenheilkunde, 210(5), 1997, pp. 329-331
REFINED LOCALIZATION OF THE CONGENITAL ACULEIFORM CATARACT
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
PHENOTYPIC VARIABILITY AND REACTIVATION PATTERNS OF RETINOMA
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
STUDY OF CRYSTALLINE GENES IN AN AUTOSOMAL RECESSIVE CATARACT PHENOTYPE
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
MEDULLO-EPITHELIOMA - 3 CASE-REPORTS
Authors: BALMER A MUNIER F UFFER S ZOGRAFOS L GAILLOUD C
Citation: A. Balmer et al., MEDULLO-EPITHELIOMA - 3 CASE-REPORTS, Klinische Monatsblatter fur Augenheilkunde, 208(5), 1996, pp. 377-380
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
REGRESSIVE BILATERAL RETINOBLASTOMA - CLI NICAL AND GENETIC-STUDY - ACASE-REPORT
Authors: MARRAKCHI S BOUGUILA H GHORBAL M BENOSMAN N MUNIER F AYED S
Citation: S. Marrakchi et al., REGRESSIVE BILATERAL RETINOBLASTOMA - CLI NICAL AND GENETIC-STUDY - ACASE-REPORT, Journal francais d'ophtalmologie, 18(5), 1995, pp. 390-395
PREFERENTIAL TRANSMISSION OF MUTANT RETINOBLASTOMA GENE BY AFFECTED FATHERS
Authors: WANG MX MUNIER F SHIELDS JA DONOSO LA
Citation: Mx. Wang et al., PREFERENTIAL TRANSMISSION OF MUTANT RETINOBLASTOMA GENE BY AFFECTED FATHERS, Investigative ophthalmology & visual science, 36(4), 1995, pp. 774-774
NEW TUMORS IN HEREDITARY RETINOBLASTOMA
Authors: BALMER A MUNIER F GAILLOUD C UFFER S VANMELLE G
Citation: A. Balmer et al., NEW TUMORS IN HEREDITARY RETINOBLASTOMA, Klinische Monatsblatter fur Augenheilkunde, 206(5), 1995, pp. 328-331
EFFICIENCY OF MOLECULAR-BASED DIAGNOSIS I N 15 RETINOBLASTOMA FAMILIES
Authors: LENDI B PESCIA G THONNEY F BALMER A MUNIER F
Citation: B. Lendi et al., EFFICIENCY OF MOLECULAR-BASED DIAGNOSIS I N 15 RETINOBLASTOMA FAMILIES, Klinische Monatsblatter fur Augenheilkunde, 206(5), 1995, pp. 336-338
FAMILIAL UVEAL MELANOMA
Authors: BERCHER L MUNIER F ZOGRAFOS L SCHORDERET D EGGER E CHAMOT L
Citation: L. Bercher et al., FAMILIAL UVEAL MELANOMA, Klinische Monatsblatter fur Augenheilkunde, 206(5), 1995, pp. 384-387
A GENETIC-ANALYSIS MODEL TO DETERMINE THE PROBABILITY OF LOW-PENETRANT INHERITANCE VERSUS FORTUITOUS AGGREGATION OF SPORADIC CASES IN RETINOBLASTOMA
Authors: WANG MX WANG MY MUNIER F UITTO JJ SHIELDS JA DONOSO LA
Citation: Mx. Wang et al., A GENETIC-ANALYSIS MODEL TO DETERMINE THE PROBABILITY OF LOW-PENETRANT INHERITANCE VERSUS FORTUITOUS AGGREGATION OF SPORADIC CASES IN RETINOBLASTOMA, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1263-1263
UNUSUAL PRESENTING SIGNS OF RETINOBLASTOM A
Authors: BALMER A GAILLOUD C MUNIER F LENDI B UFFER S
Citation: A. Balmer et al., UNUSUAL PRESENTING SIGNS OF RETINOBLASTOM A, Klinische Monatsblatter fur Augenheilkunde, 204(5), 1994, pp. 313-315
RETINOBLASTOMA - UNUSUAL WARNING AND CLINICAL SIGNS
Authors: BALMER A GAILLOUD C MUNIER F UFFER S GUEXCROSIER Y
Citation: A. Balmer et al., RETINOBLASTOMA - UNUSUAL WARNING AND CLINICAL SIGNS, Ophthalmic paediatrics and genetics, 14(1), 1993, pp. 33-38
MOLECULAR-GENETICS OF RETINOBLASTOMA
Authors: ZHANG K WANG MX MUNIER F ROTH D MASTRANGELO D CHUNG S SHIELDS JA DONOSO LA
Citation: K. Zhang et al., MOLECULAR-GENETICS OF RETINOBLASTOMA, International ophthalmology clinics, 33(3), 1993, pp. 53-65
Risultati: 1-25 | 26-26