Pages that link to "Q46818410"

The following pages link to Variable expressivity of autosomal dominant microcornea with cataract (Q46818410):

Displaying 16 items.

• Heterogeneity in dominant anterior segment malformations (Q33649092) (← links)
• An unusual pedigree with microcornea-cataract syndrome. (Q33682635) (← links)
• Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome. (Q34164340) (← links)
• The Peters' plus syndrome: a review (Q34525318) (← links)
• The morphology and natural history of childhood cataracts (Q35103616) (← links)
• Novel human CRYGD rare variant in a Brazilian family with congenital cataract (Q35175320) (← links)
• Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family (Q35590740) (← links)
• Cataract surgery for tilted lens in peters' anomaly type 2 (Q37251280) (← links)
• Bilateral congenital dentiform cataract and extreme microcornea in eyes with uveal colobomas and persistent hyperplastic primary vitreous (Q37319922) (← links)
• Genetic modifiers as relevant biological variables of eye disorders (Q39290939) (← links)
• Genetics of aniridia and anterior segment dysgenesis (Q39720018) (← links)
• Mapping X-linked ophthalmic diseases. IV. Provisional assignment of the locus for X-linked congenital cataracts and microcornea (the Nance-Horan syndrome) to Xp22.2-p22.3. (Q41756361) (← links)
• Autosomal dominant congenital cataract. Interocular phenotypic variability. (Q47231040) (← links)
• Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis (Q55984321) (← links)
• Infantile cataracts (Q71305130) (← links)
• Confirmation of the colobomatous macrophthalmia with microcornea syndrome: Report of another family (Q74329952) (← links)