Frontiers | Novel GJA1/Cx43 Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms
What is Oculodentodigital Dysplasia?
Oculo-Dento-Digital Dysplasia
Oculodentodigital dysplasia: MedlinePlus Genetics
Patient Reviews | Modern Dental Studio - East Brunswick NJ
Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
The Bardet–Biedl and orofacial digital type 1 ciliopathies | Polycystic Kidney Disease: from Bench to Bedside
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Oculodentodigital dysplasia: MedlinePlus Genetics
Midwestern University Clinics Illinois Dental News | MWU IL Dental Clinic
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a) Facial dysmorphism typical of ODDD present in proband 1 at the age... | Download Scientific Diagram
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Dental Problems in Childhood Cancer Survivors - Together
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Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia - ScienceDirect
Oculodentodigital dysplasia: MedlinePlus Genetics
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
