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Oculo-Dento-Digital Dysplasia
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
What is Oculodentodigital Dysplasia?
John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging - ScienceDirect
IJERPH | Free Full-Text | Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
What is Oculodentodigital Dysplasia?
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia - ScienceDirect
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
Oculodentodigital dysplasia: MedlinePlus Genetics
Oral-facial-digital syndrome: MedlinePlus Genetics
Patient Reviews | Modern Dental Studio - East Brunswick NJ
Oculodentodigital Syndrome - NFED
rare_diseases_in_pediatric_anesthesia
Midwestern University Clinics Illinois Dental News | MWU IL Dental Clinic
Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
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What is Oculodentodigital Dysplasia?
Frontiers | Novel GJA1/Cx43 Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms
A Case of Lacrimo-Auriculo-Dento-Digital Syndrome with Multiple Congenitally Missing Teeth
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Frontiers | Novel GJA1/Cx43 Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms
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