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Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
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Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
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Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
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A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
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PDF] Three novel GJA1 missense substitutions resulting in oculo-dento- digital dysplasia (ODDD) - Further extension of the mutational spectrum
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John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
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Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
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Facial photograph of a patient with oculodentodigital dysplasia; note... | Download Scientific Diagram
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Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature | SpringerLink
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