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Geographic distribution and regional origin of 272 cystic fibrosis in European populations
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Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.
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Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON)
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Proximal deletion of chromosome-21 confirmed by in-situ hybridization and molecular studies.
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Features of mitochondrial DNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.