John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
Dental Problems in Childhood Cancer Survivors - Together
The Bardet–Biedl and orofacial digital type 1 ciliopathies | Polycystic Kidney Disease: from Bench to Bedside
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
IJERPH | Free Full-Text | Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
Radiographic diagnosis of a rare case of oculo-dento-digital dysplasia | Parashari | South African Journal of Radiology
Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
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Oculodentodigital dysplasia: MedlinePlus Genetics
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
What is Oculodentodigital Dysplasia?
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
PDF) Neurological manifestations of the oculodentodigital dysplasia syndrome
A Case of Lacrimo-Auriculo-Dento-Digital Syndrome with Multiple Congenitally Missing Teeth
Oculodentodigital dysplasia: MedlinePlus Genetics
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging - ScienceDirect
Oculodentodigital dysplasia: MedlinePlus Genetics
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
Orthodontic treatment of a patient with oral-facial-digital syndrome | Pocket Dentistry
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia - ScienceDirect
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature | Semantic Scholar
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
