Pages that link to "Q28297543"

The following pages link to Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation family (Q28297543):

Displaying 13 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)
• GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype (Q37429017) (← links)
• A novel GJA1 missense mutation in a Polish child with oculodentodigital dysplasia. (Q39894832) (← links)
• Oculodentodigital Dysplasia: Ulnar-Sided Syndactyly and Its Associated Disorders (Q44121056) (← links)
• A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel (Q48165333) (← links)
• A Novel GJA1 Mutation in Oculodentodigital Dysplasia with Progressive Spastic Paraplegia and Sensory Deficits (Q48731309) (← links)
• Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family (Q49033964) (← links)
• Evidence for genetic anticipation in the oculodentodigital syndrome (Q57925703) (← links)
• [Progressive spastic paraplegia as a presentation of oculodentodigital syndrome] (Q76378544) (← links)
• Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases (Q92134278) (← links)