AAAAAA

   
Results: 1-24 |
Results: 24
EVIDENCE FOR GENETIC-HETEROGENEITY IN X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS
Authors: BOYCOTT KM PEARCE WG MUSARELLA MA WELEBER RG MAYBAUM TA BIRCH DG MIYAKE Y YOUNG RSL BECHHANSEN NT
Citation: Km. Boycott et al., EVIDENCE FOR GENETIC-HETEROGENEITY IN X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS, American journal of human genetics, 62(4), 1998, pp. 865-875
LOSS-OF-FUNCTION MUTATIONS IN A CALCIUM-CHANNEL ALPHA(1)-SUBUNIT GENEIN XP11.23 CAUSE INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS
Authors: BECHHANSEN NT NAYLOR MJ MAYBAUM TA PEARCE WG KOOP B FISHMAN GA METS M MUSARELLA MA BOYCOTT KM
Citation: Nt. Bechhansen et al., LOSS-OF-FUNCTION MUTATIONS IN A CALCIUM-CHANNEL ALPHA(1)-SUBUNIT GENEIN XP11.23 CAUSE INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS, Nature genetics, 19(3), 1998, pp. 264-267
MUTATION IN THE RIEG1 GENE IN PATIENTS WITH IRIDOGONIODYSGENESIS SYNDROME
Authors: KULAK SC KOZLOWSKI K SEMINA EV PEARCE WG WALTER MA
Citation: Sc. Kulak et al., MUTATION IN THE RIEG1 GENE IN PATIENTS WITH IRIDOGONIODYSGENESIS SYNDROME, Human molecular genetics (Print), 7(7), 1998, pp. 1113-1117
LOCALIZATION OF A GENE FOR INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS TO THE INTERVAL BETWEEN DXS6849 AND DXS8023 IN XP11.23
Authors: BECHHANSEN NT BOYCOTT KM GRATTON KJ BOSS DA FIELD LL PEARCE WG
Citation: Nt. Bechhansen et al., LOCALIZATION OF A GENE FOR INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS TO THE INTERVAL BETWEEN DXS6849 AND DXS8023 IN XP11.23, Human genetics, 103(2), 1998, pp. 124-130
AXENFELD-RIEGER ANOMALY MAPS TO 6P25
Authors: GOULD DB MEARS AJ PEARCE WG WALTER MA
Citation: Db. Gould et al., AXENFELD-RIEGER ANOMALY MAPS TO 6P25, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3728-3728
EVIDENCE FOR GENETIC-HETEROGENEITY IN X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS
Authors: BECHHANSEN NT PEARCE WG MUSARELLA MA WELEBER RG MAYBAUM TA BIRCH DG MIYAKE Y BOYCOTT KM
Citation: Nt. Bechhansen et al., EVIDENCE FOR GENETIC-HETEROGENEITY IN X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS, American journal of human genetics, 61(4), 1997, pp. 1339-1339
PHYSICAL AND GENETIC-MAPPING OF THE IGDA LOCUS AT 6P25
Authors: MEARS AJ COLLINS C MIRZAYANS F MYAMBO K WERNICK M KUO WL PEARCE WG WALTER MA
Citation: Aj. Mears et al., PHYSICAL AND GENETIC-MAPPING OF THE IGDA LOCUS AT 6P25, American journal of human genetics, 61(4), 1997, pp. 1665-1665
MUTATION OF THE RIEG1 GENE IN PATIENTS WITH IRIDOGONIODYSGENESIS SYNDROME
Authors: KULAK SC KOZLOWSKI K SEMINA EV PEARCE WG WALTER MA
Citation: Sc. Kulak et al., MUTATION OF THE RIEG1 GENE IN PATIENTS WITH IRIDOGONIODYSGENESIS SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1976-1976
AUTOSOMAL-DOMINANT AXENFELD-RIEGER ANOMALY MAPS TO 6P25
Authors: GOULD DB MEARS AJ PEARCE WG WALTER MA
Citation: Db. Gould et al., AUTOSOMAL-DOMINANT AXENFELD-RIEGER ANOMALY MAPS TO 6P25, American journal of human genetics, 61(3), 1997, pp. 765-768
IDENTIFICATION OF THE HUMAN CHROMOSOMAL REGION CONTAINING THE IRIDOGONIODYSGENESIS ANOMALY LOCUS BY GENOMIC-MISMATCH SCANNING
Authors: MIRZAYANS F MEARS AJ GUO SW PEARCE WG WALTER MA
Citation: F. Mirzayans et al., IDENTIFICATION OF THE HUMAN CHROMOSOMAL REGION CONTAINING THE IRIDOGONIODYSGENESIS ANOMALY LOCUS BY GENOMIC-MISMATCH SCANNING, American journal of human genetics, 61(1), 1997, pp. 111-119
AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS AND AXENFELD-RIEGER SYNDROME ARE GENETICALLY DISTINCT
Authors: WALTER MA MIRZAYANS F MEARS AJ HICKEY K PEARCE WG
Citation: Ma. Walter et al., AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS AND AXENFELD-RIEGER SYNDROME ARE GENETICALLY DISTINCT, Ophthalmology, 103(11), 1996, pp. 1907-1915
IRIDOGONIODYSGENESIS IS GENETICALLY DISTINCT FROM AXENFELD-RIEGER SYNDROME
Authors: MEARS AJ PEARCE WG MIRZAYANS F WALTER MA
Citation: Aj. Mears et al., IRIDOGONIODYSGENESIS IS GENETICALLY DISTINCT FROM AXENFELD-RIEGER SYNDROME, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2077-2077
AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS ANOMALY MAPS TO 6P25
Authors: MEARS AJ MIRZAYANS F GOULD DB PEARCE WG WALTER MA
Citation: Aj. Mears et al., AUTOSOMAL-DOMINANT IRIDOGONIODYSGENESIS ANOMALY MAPS TO 6P25, American journal of human genetics, 59(6), 1996, pp. 1321-1327
X-LINKED RETINITIS-PIGMENTOSA - REEVALUATION OF FUNDUS FINDINGS AND THE USE OF HAPLOTYPE ANALYSIS IN CLARIFICATION OF CARRIER FEMALE STATUS
Authors: BECHHANSEN NT PEARCE WG
Citation: Nt. Bechhansen et Wg. Pearce, X-LINKED RETINITIS-PIGMENTOSA - REEVALUATION OF FUNDUS FINDINGS AND THE USE OF HAPLOTYPE ANALYSIS IN CLARIFICATION OF CARRIER FEMALE STATUS, Ophthalmic genetics, 16(3), 1995, pp. 113-118
AUTOSOMAL-DOMINANT KERATITIS - A POSSIBLE ANIRIDIA VARIANT
Authors: PEARCE WG MIELKE BW HASSARD DTR CLIMENHAGA HW CLIMENHAGA DB HODGES EJ
Citation: Wg. Pearce et al., AUTOSOMAL-DOMINANT KERATITIS - A POSSIBLE ANIRIDIA VARIANT, Canadian journal of ophthalmology, 30(3), 1995, pp. 131-137
MUTATION OF THE PAX6 GENE IN PATIENTS WITH AUTOSOMAL-DOMINANT KERATITIS
Authors: WALTER MA MIRZAYANS F MACDONALD IM PEARCE WG
Citation: Ma. Walter et al., MUTATION OF THE PAX6 GENE IN PATIENTS WITH AUTOSOMAL-DOMINANT KERATITIS, American journal of human genetics, 57(4), 1995, pp. 236-236
DEFINITION OF A 14 CM CRITICAL REGION FOR AXENFELD-RIEGER SYNDROME ATCHROMOSOME 4Q25-27
Authors: MIRZAYANS F TONK V KUKOLICH MK PEARCE WG WALTER MA
Citation: F. Mirzayans et al., DEFINITION OF A 14 CM CRITICAL REGION FOR AXENFELD-RIEGER SYNDROME ATCHROMOSOME 4Q25-27, American journal of human genetics, 57(4), 1995, pp. 1137-1137
MUTATION OF THE PAX6 GENE IN PATIENTS WITH AUTOSOMAL-DOMINANT KERATITIS
Authors: MIRZAYANS F PEARCE WG MACDONALD IM WALTER MA
Citation: F. Mirzayans et al., MUTATION OF THE PAX6 GENE IN PATIENTS WITH AUTOSOMAL-DOMINANT KERATITIS, American journal of human genetics, 57(3), 1995, pp. 539-548
HYBRID AND MEIOTIC MAPPING AND CONSTRUCTION OF A YAC CONTIG IN THE XP11 REGION
Authors: BECHHANSEN NT GRATTON KJ MOORE BJ HALLEY G PEARCE WG BOYCOTT KM
Citation: Nt. Bechhansen et al., HYBRID AND MEIOTIC MAPPING AND CONSTRUCTION OF A YAC CONTIG IN THE XP11 REGION, Cytogenetics and cell genetics, 67(4), 1994, pp. 358-358
VARIABILITY OF IRIS DEFECTS IN AUTOSOMAL-DOMINANT ANIRIDIA
Authors: PEARCE WG
Citation: Wg. Pearce, VARIABILITY OF IRIS DEFECTS IN AUTOSOMAL-DOMINANT ANIRIDIA, Canadian journal of ophthalmology, 29(1), 1994, pp. 25-29
INHERITED IRIDOGONIODYSGENESIS - REPLY
Authors: MACDONALD IM PEARCE WG
Citation: Im. Macdonald et Wg. Pearce, INHERITED IRIDOGONIODYSGENESIS - REPLY, Ophthalmology, 100(11), 1993, pp. 1598-1599
INCIDENCE OF ACCOMMODATIVE IMPAIRMENT FOLLOWING TRAUMATIC HYPHEMA
Authors: THERIAULT FA PEARCE WG
Citation: Fa. Theriault et Wg. Pearce, INCIDENCE OF ACCOMMODATIVE IMPAIRMENT FOLLOWING TRAUMATIC HYPHEMA, Canadian journal of ophthalmology, 28(6), 1993, pp. 263-265
UNEXPECTED STEREOACUITY FOLLOWING SURGICAL-CORRECTION OF LONG-STANDING HORIZONTAL STRABISMUS
Authors: BALL A DRUMMOND GT PEARCE WG
Citation: A. Ball et al., UNEXPECTED STEREOACUITY FOLLOWING SURGICAL-CORRECTION OF LONG-STANDING HORIZONTAL STRABISMUS, Canadian journal of ophthalmology, 28(5), 1993, pp. 217-220
LOCALIZATION OF THE GENE FOR X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS WITHIN THE XP11 REGION AND CANDIDATE GENE ANALYSIS USING THE DIDEOXY FINGERPRINTING METHOD
Authors: BECHHANSEN NT FIELD LL GRATTON K PEARCE WG
Citation: Nt. Bechhansen et al., LOCALIZATION OF THE GENE FOR X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS WITHIN THE XP11 REGION AND CANDIDATE GENE ANALYSIS USING THE DIDEOXY FINGERPRINTING METHOD, American journal of human genetics, 53(3), 1993, pp. 973-973
Risultati: 1-24 |