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Results: 1-15 |
Results: 15
DOMINANT INHERITANCE OF OPTIC PITS
Authors: RAGGE NK RAVINE D WILKIE AOM
Citation: Nk. Ragge et al., DOMINANT INHERITANCE OF OPTIC PITS, American journal of ophthalmology, 125(1), 1998, pp. 124-124
THE OCULAR PRESENTATION OF NEUROFIBROMATOSIS-2
Authors: RAGGE NK BASER ME RICCARDI VM FALK RE
Citation: Nk. Ragge et al., THE OCULAR PRESENTATION OF NEUROFIBROMATOSIS-2, Eye, 11, 1997, pp. 12-18
DOMINANT COLOBOMA-MICROPHTHALMOS SYNDROME-ASSOCIATED WITH SENSORINEURAL HEARING-LOSS, HEMATURIA, AND CLEFT LIP PALATE/
Authors: RAVINE D RAGGE NK STEPHENS D OLDRIDGE M WILKIE AOM
Citation: D. Ravine et al., DOMINANT COLOBOMA-MICROPHTHALMOS SYNDROME-ASSOCIATED WITH SENSORINEURAL HEARING-LOSS, HEMATURIA, AND CLEFT LIP PALATE/, American journal of medical genetics, 72(2), 1997, pp. 227-236
IRIS MAMMILLATIONS - SIGNIFICANCE AND ASSOCIATIONS
Authors: RAGGE NK ACHESON J MURPHREE AL
Citation: Nk. Ragge et al., IRIS MAMMILLATIONS - SIGNIFICANCE AND ASSOCIATIONS, Eye, 10, 1996, pp. 86-91
PHENOTYPIC VARIABILITY IN MONOZYGOTIC TWINS WITH NEUROFIBROMATOSIS-2
Authors: BASER ME RAGGE NK RICCARDI VM JANUS T GANTZ B PULST SM
Citation: Me. Baser et al., PHENOTYPIC VARIABILITY IN MONOZYGOTIC TWINS WITH NEUROFIBROMATOSIS-2, American journal of medical genetics, 64(4), 1996, pp. 563-567
PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS
Authors: BASER ME MAUTNER VF RAGGE NK NECHIPORUK A RICCARDI VM KLEIN J SAINZ J PULST SM
Citation: Me. Baser et al., PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS, Neurology, 47(5), 1996, pp. 1269-1277
VONHIPPEL-LINDAU SYNDROME - CLINICO-MOLECULAR STUDY OF A LARGE PEDIGREE
Authors: RAGGE NK CROSSEY PA MAHER ER MURPHREE AL FALK RE
Citation: Nk. Ragge et al., VONHIPPEL-LINDAU SYNDROME - CLINICO-MOLECULAR STUDY OF A LARGE PEDIGREE, Investigative ophthalmology & visual science, 36(4), 1995, pp. 1057-1057
OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2
Authors: RAGGE NK BASER ME KLEIN J NECHIPORUK A SAINZ J PULST SM RICCARDI VM
Citation: Nk. Ragge et al., OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2, American journal of ophthalmology, 120(5), 1995, pp. 634-641
MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS
Authors: SAINZ J HUYNH DP FIGUEROA K RAGGE NK BASER ME PULST SM
Citation: J. Sainz et al., MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS, Human molecular genetics, 3(6), 1994, pp. 885-891
NEUROOPHTHALMOLOGY IN THE EASTERN-EUROPEAN COUNTRIES
Authors: PAPAKOSTOPOULOS D DONOVAN RML RAGGE NK
Citation: D. Papakostopoulos et al., NEUROOPHTHALMOLOGY IN THE EASTERN-EUROPEAN COUNTRIES, Neuro-ophthalmology, 14(2), 1994, pp. 75-77
ANCIENT NEUROFIBROMATOSIS
Authors: RAGGE NK MUNIER FL
Citation: Nk. Ragge et Fl. Munier, ANCIENT NEUROFIBROMATOSIS, Nature, 368(6474), 1994, pp. 815-815
LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22
Authors: SAINZ J BASER ME RAGGE NK NELSON RA PULST SM
Citation: J. Sainz et al., LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22, Archives of otolaryngology, head & neck surgery, 119(12), 1993, pp. 1285-1288
CLINICAL AND GENETIC PATTERNS OF NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2
Authors: RAGGE NK
Citation: Nk. Ragge, CLINICAL AND GENETIC PATTERNS OF NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2, British journal of ophthalmology, 77(10), 1993, pp. 662-672
PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS
Authors: PULST SM BASER ME MAUTNER V SAINZ J NECHIPORUK A KLEIN J NELSON RA RAGGE NK RICCARDI VM
Citation: Sm. Pulst et al., PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS, American journal of human genetics, 53(3), 1993, pp. 488-488
STICKLER HEREDITARY ARTHROOPHTHALMOPATHY - A HETEROGENEOUS PHENOTYPE
Authors: RAGGE NK COHN DH WILKIN DJ CHIN R MURPHREE AL FALK RE
Citation: Nk. Ragge et al., STICKLER HEREDITARY ARTHROOPHTHALMOPATHY - A HETEROGENEOUS PHENOTYPE, American journal of human genetics, 53(3), 1993, pp. 490-490
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