Pages that link to "Q57925703"
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The following pages link to Evidence for genetic anticipation in the oculodentodigital syndrome (Q57925703):
Displaying 7 items.
- Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia (Q24610890) (← links)
- Gap junctions couple astrocytes and oligodendrocytes (Q24645936) (← links)
- Gap junctions in inherited human disorders of the central nervous system (Q26823332) (← links)
- Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature (Q31111437) (← links)
- A novel truncation mutation in GJA1 associated with open angle glaucoma and microcornea in a large Chinese family (Q35863038) (← links)
- Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia (Q38862310) (← links)
- Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases (Q92134278) (← links)