What is Oculodentodigital Dysplasia?
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Oculodentodigital dysplasia Doshi DC, Limdi PK, Parekh NV, Gohil NR - Indian J Ophthalmol
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene - ScienceDirect
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. - Document - Gale Academic OneFile
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging - ScienceDirect
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
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Oculodentodigital Dysplasia | Neurology
What is Oculodentodigital Dysplasia?
Oculodentodigital dysplasia: plastic treatments and self-esteem estimation | SpringerLink
Oculodentodigital Dysplasia | Hereditary Ocular Diseases
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
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
Oculodentodigital dysplasia: plastic treatments and self-esteem estimation | SpringerLink
![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
Oculodentodigital dysplasia: MedlinePlus Genetics
IJERPH | Free Full-Text | Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature | SpringerLink
