OCULODENTODIGITAL DYSPLASIA SYNDROME <i>Report of Four Cases</i>
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
Disorders of the eye as a whole | Ento Key
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. - Document - Gale Academic OneFile
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature | Semantic Scholar
Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Oculodentodigital dysplasia: plastic treatments and self-esteem estimation | SpringerLink
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
Oculodentodigital dysplasia: MedlinePlus Genetics
Oculodentodigital dysplasia
Oculodentodigital dysplasia: MedlinePlus Genetics
Oculodentodigital Dysplasia Diagnosed from Severe Hypotrichosis | HTML | Acta Dermato-Venereologica
Journal of Movement Disorders
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Oculodentodigital dysplasia. - Abstract - Europe PMC
Oculodentodigital Syndrome - NFED
1'- & 16
Oculo-Dento-Digital Dysplasia (ODDD) | ACNR
What is Oculodentodigital Dysplasia?
What is Oculodentodigital Dysplasia?
