Françoise Meire
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Autosomal dominant congenital miosis with megalocornea.
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The Hallerman-Strciff syndrome
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Optic atrophy as a complication of neonatal alloimmune thrombocytopenia
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Hereditary ectopia lentis
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X-linked megalocomea. Ocular findings and linkage analysis.
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Retinal manifestations in fibromuscular dysplasia
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Ocular manifestations of congenital Marfan syndrome with contractures.
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DNA variants: A third allele of the Pstl RFLP at DXS94
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PERSISTING CHLOROQUINE-INDUCED MYASTHENIA.
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Optic nerve hypoplasia. Ophthalmol., nr. 105,1998, pp. 4-5.