Ophthalmic Paediatrics and Genetics

Titel Veröffentlichungsdatum Sprache Zitate
Microphthalmia-Congenital Anterior Polar Cataract: An Autosomal Dominant Syndrome1985/01/01English5
Recessively Inherited, Simple Optic Atrophy -Does it Exist?1992/01/01English5
Demonstration of Bias in Series of Retinoblastoma1989/01/01English5
Confirmation of X-Linked Inheritance and Provisional Mapping of the Keratosis Follicularis Spinulosa Decalvans Gene on XP in a Large Dutch Family1992/01/01English5
Mitochondrial DNA Analysis as a Diagnostic Tool in Singleton Cases of Leber's Hereditary Optic Neuropathy1993/01/01English5
Retinal Angioma and Juvenile Sex-Linked Retinoschisis1992/01/01English5
Ultrastructure of the skin of human albinos1983/01/01English4
Italian register for retinoblastoma Pros and cons of a retrospective statistical study1991/01/01English4
Incidence of retinoblastoma in Nagasaki Prefecture, Japan1991/01/01English4
Heterozygote detection in X-linked recessive incomplete achromatopsia1988/01/01English4
A hereditary syndrome with retinopathy and ataxia or deafness in two consanguineous brothers1991/01/01English4
The aniridia-Wilms' tumor syndrome and other associations of aniridia1982/01/01English4
A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance1990/01/01English4
Corneal alpha-galactosidase deficiency in macular corneal dystrophy1985/01/01English4
X-linked cataract1982/01/01English4
The nutritional sources and limits of intraocular retinoblastoma growth1987/01/01English4
Superoxide dismutase activity and reduced glutathione content in cataractous lens of patients with glucose-6-phosphate dehydrogenase deficiency1987/01/01English4
Hereditary congenital nystagmus A Japanese pedigree1986/01/01English4
Normal and abnormal visual field maps in albinos: Central effects of non-matching maps1990/01/01English4
Acrofacial dysostosis of Nager and ocular abnormalities1986/01/01English4
Seckel's Syndrome with Pseudopolycoria1985/01/01English4
Assessment of binocular function during infancy1983/01/01English4
Dominant optic atrophy with sensorineural hearing loss1982/01/01English4
Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis Problems due to genetic heterogeneity1991/01/01English4
Tapetoretinal degeneration associated with multisystem abnormalities: A case report1986/01/01English4
Microphthalmos in a family1985/01/01English4
Congenital optic disc deformities: A clinical approach1985/01/01English4
Studies in dominant optic atrophy1985/01/01English4
Visual acuity of infants and children with retinal degenerations1985/01/01English4
Did atomic bomb radiation influence the incidence of retinoblastoma in Nagasaki and Hiroshima?1993/01/01English4