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Facial photograph of a patient with oculodentodigital dysplasia; note... | Download Scientific Diagram
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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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Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature | SpringerLink
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Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene - ScienceDirect
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Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
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Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging - ScienceDirect
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Frontiers | A Novel Homozygous Variant in GJA1 Causing a Hallermann-Streiff/ Oculodentodigital Dysplasia Overlapping Phenotype: A Clinical Report
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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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