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Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD) - ScienceDirect
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
Two novel GJA1 variants in oculodentodigital dysplasia - Pace - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Figure 2 from Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imaging. | Semantic Scholar
What is Oculodentodigital Dysplasia?
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene - International Journal of Oral and Maxillofacial Surgery
Oculodentodigital dysplasia: plastic treatments and self-esteem estimation | SpringerLink
Clinical manifestations of oculodentodigital dysplasia Kayalvizhi G, Subramaniyan B, Suganya G - J Indian Soc Pedod Prev Dent
Journal of Movement Disorders
What is Oculodentodigital Dysplasia?
▷ Is Oculo-Dento-Digital Dysplasia hereditary?
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome | Journal of Medical Genetics
Frontiers | A Novel Homozygous Variant in GJA1 Causing a Hallermann-Streiff/ Oculodentodigital Dysplasia Overlapping Phenotype: A Clinical Report
Oculodentodigital dysplasia: plastic treatments and self-esteem estimation | SpringerLink
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
Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
Dental management of oculodentodigital dysplasia: a case report. | Semantic Scholar
a) Facial dysmorphism typical of ODDD present in proband 1 at the age... | Download Scientific Diagram
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature | Semantic Scholar
OCULODENTODIGITAL DYSPLASIA SYNDROME <i>Report of Four Cases</i>
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) | Eye
PDF) Neurological manifestations of the oculodentodigital dysplasia syndrome
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. - Document - Gale Academic OneFile
Oculodentodigital dysplasia. - Abstract - Europe PMC