Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Frontiers | Novel GJA1/Cx43 Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Midwestern University Clinics Illinois Dental News | MWU IL Dental Clinic
Oculodentodigital dysplasia: MedlinePlus Genetics
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia - ScienceDirect
What is Oculodentodigital Dysplasia?
Radiographic diagnosis of a rare case of oculo-dento-digital dysplasia | Parashari | South African Journal of Radiology
a) Facial dysmorphism typical of ODDD present in proband 1 at the age... | Download Scientific Diagram
Oral-facial-digital syndrome: MedlinePlus Genetics
Dental Problems in Childhood Cancer Survivors - Together
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
A Case of Lacrimo-Auriculo-Dento-Digital Syndrome with Multiple Congenitally Missing Teeth
Our Christmas Wish
Patient Reviews | Modern Dental Studio - East Brunswick NJ
rare_diseases_in_pediatric_anesthesia
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
Our Christmas Wish
The Bardet–Biedl and orofacial digital type 1 ciliopathies | Polycystic Kidney Disease: from Bench to Bedside
