Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
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Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
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Oculodentodigital dysplasia: MedlinePlus Genetics
a) Facial dysmorphism typical of ODDD present in proband 1 at the age... | Download Scientific Diagram
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia - ScienceDirect
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Dental Problems in Childhood Cancer Survivors - Together
PDF) Neurological manifestations of the oculodentodigital dysplasia syndrome
Oculodentodigital dysplasia: MedlinePlus Genetics
Midwestern University Clinics Illinois Dental News | MWU IL Dental Clinic
John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis