about
Peters'-plus: a new syndromeBest's vitelliform dystrophy.The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndrome.A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report).Incidence of retinoblastoma in Nagasaki Prefecture, Japan.Retinoblastoma in the first year of life.Preferential looking--clinical lessons.Update of sporadic microphthalmos and coloboma. Non-inherited anomalies.Mapping the eye diseases.Investigation of disease mechanisms in retinitis pigmentosa.Aspects of albinism.POSSUM: the microcomputer laser-videodisk syndrome information system.A new look at the management of the oculo-mandibulo-facial syndrome.Iris cysts in three generations conveyed by means of a genetic process connected with sex.A case of retinitis pigmentosa associated with Coats' syndrome.Chemotherapy for retinoblastoma: where do we go from here? A review of published literature and meeting abstracts, including discussions during the Vth International Symposium on Retinoblastoma, October 1990.X-linked megalocornea. Ocular findings and linkage analysis.An update on microphthalmos and coloboma. A brief survey of genetic disorders with microphthalmos and coloboma.Recurrent and new tumours during conservative treatment of bilateral retinoblastoma.Mapping of the X-linked recessive retinitis pigmentosa gene. A review.Comparative genetics of albinism.Usher's syndrome.The Morning Glory syndrome associated with sphenoethmoidal encephalocele.Retinal image quality in albinos. A review.Normal and abnormal visual field maps in albinos. Central effects of non-matching maps.Walker-Warburg syndrome. Case report and literature review.Retinoblastoma. Interphotoreceptor retinoid binding protein mRNA analysis by polymerase chain reaction.Aniridia, Wilms' tumor and human chromosome 11.One hundred years of retinoblastoma research. From the clinic to the gene and back again.Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome.Sex chromosome aneuploidy and Bardet-Biedl syndrome.Visual acuity of infants and children with retinal degenerations.Immunohistochemistry of retinoblastoma. A review.Experimental models of anterior segment dysgenesis.Constitutional karyotype in retinoblastoma. Case report and review of literature.Papillo-renal syndrome. An inherited association of optic disc dysplasia and renal disease. Report and review of the literature.Diagnostic morphology of human eye-related storage disorders.Leber's hereditary optic atrophy.Congenital and developmental cataracts and multimalformation syndromes.
P1433
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P1433
description
revista científica
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revue scientifique
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rivista scientifica
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scientific journal
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wetenschappelijk tijdschrift
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wissenschaftliche Fachzeitschrift
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науковий журнал
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name
Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
@fr
Ophthalmic Paediatrics and Genetics
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Ophthalmic paediatrics and genetics
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type
label
Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
@en
Ophthalmic Paediatrics and Genetics
@es
Ophthalmic Paediatrics and Genetics
@fr
Ophthalmic Paediatrics and Genetics
@it
Ophthalmic paediatrics and genetics
@nl
altLabel
Ophthalmic Paediatr Genet
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prefLabel
Ophthalmic Paediatrics and Genetics
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Ophthalmic Paediatrics and Genetics
@de
Ophthalmic Paediatrics and Genetics
@en
Ophthalmic Paediatrics and Genetics
@es
Ophthalmic Paediatrics and Genetics
@fr
Ophthalmic Paediatrics and Genetics
@it
Ophthalmic paediatrics and genetics
@nl
P3181
P1055
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P1476
Ophthalmic Paediatrics and Genetics
@en