John Libbey Eurotext - European Journal of Dermatology - A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
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IJERPH | Free Full-Text | Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
What is Oculodentodigital Dysplasia?
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
Oculodentodigital dysplasia Doshi DC, Limdi PK, Parekh NV, Gohil NR - Indian J Ophthalmol
Two novel GJA1 variants in oculodentodigital dysplasia - Pace - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. - Document - Gale Academic OneFile
What is Oculodentodigital Dysplasia?
![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: plastic treatments and self-esteem estimation | SpringerLink
Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging - ScienceDirect
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
Oculodentodigital Dysplasia | Neurology
Oculodentodigital dysplasia Doshi DC, Limdi PK, Parekh NV, Gohil NR - Indian J Ophthalmol
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Oculo-Dento-Digital Dysplasia
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
OCULODENTODIGITAL DYSPLASIA SYNDROME <i>Report of Four Cases</i>
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature
Clinical manifestations of oculodentodigital dysplasia
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature | SpringerLink
