Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
Oculodentodigital dysplasia Doshi DC, Limdi PK, Parekh NV, Gohil NR - Indian J Ophthalmol
Oculodentodigital syndrome: report of a case.
Oculodentodigital dysplasia: MedlinePlus Genetics
Two novel GJA1 variants in oculodentodigital dysplasia - Pace - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![PDF] Three novel GJA1 missense substitutions resulting in oculo-dento- digital dysplasia (ODDD) - Further extension of the mutational spectrum](https://www.researchgate.net/profile/Aleksander-Jamsheer/publication/260129906/figure/fig2/AS:388412394754051@1469616139547/a-Facial-dysmorphism-typical-of-ODDD-present-in-proband-1-at-the-age-of-45-years-b_Q320.jpg "PDF] Three novel GJA1 missense substitutions resulting in oculo-dento- digital dysplasia (ODDD) - Further extension of the mutational spectrum")
PDF] Three novel GJA1 missense substitutions resulting in oculo-dento- digital dysplasia (ODDD) - Further extension of the mutational spectrum
Oculo-Dento-Digital Dysplasia
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Clinical manifestations of oculodentodigital dysplasia
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
What is Oculodentodigital Dysplasia?
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Oculodentodigital Syndrome - NFED
Oculodentodigital Dysplasia | Neurology
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. - Document - Gale Academic OneFile
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Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene - ScienceDirect
Facial photograph of a patient with oculodentodigital dysplasia; note... | Download Scientific Diagram
Oculodentodigital dysplasia: MedlinePlus Genetics
What is Oculodentodigital Dysplasia?
