Oculodentodigital Dysplasia | Neurology
Oculo-Dento-Digital Dysplasia
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
IJERPH | Free Full-Text | Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene - ScienceDirect
Oculodentodigital Syndrome - NFED
What is Oculodentodigital Dysplasia?
Oculodentodigital dysplasia: MedlinePlus Genetics
Facial photograph of a patient with oculodentodigital dysplasia; note... | Download Scientific Diagram
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
What is Oculodentodigital Dysplasia?
Oculodentodigital dysplasia: MedlinePlus Genetics
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
Two novel GJA1 variants in oculodentodigital dysplasia - Pace - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
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Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
