Pages that link to "Q37300064"

The following pages link to X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis (Q37300064):

Displaying 29 items.

• Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5. (Q24302508) (← links)
• A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy (Q24321645) (← links)
• Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity (Q28290026) (← links)
• A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13. (Q28348819) (← links)
• Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous (Q33596248) (← links)
• A fetus with an X;1 balanced reciprocal translocation and eye disease (Q33677139) (← links)
• Familial exudative vitreoretinopathy (Q34211264) (← links)
• The molecular biology of Norrie's disease (Q34317165) (← links)
• A novel nonsense mutation in the NDP gene in a Chinese family with Norrie disease (Q34410786) (← links)
• Familial exudative vitreoretinopathy and related retinopathies (Q34905378) (← links)
• Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigree (Q35314112) (← links)
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree (Q35592879) (← links)
• Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5 (Q35762505) (← links)
• The Wnt signaling pathway in familial exudative vitreoretinopathy and Norrie disease (Q37039789) (← links)
• Manifesting heterozygosity in Norrie's disease? (Q37304088) (← links)
• Canonical Wnt signaling in diabetic retinopathy. (Q39331082) (← links)
• Retinal photoreceptor dystrophies LI. Edward Jackson Memorial Lecture (Q40515350) (← links)
• Persistent Fetal Vasculature (PFV): An Integrated Interpretation of Signs and Symptoms Associated With Persistent Hyperplastic Primary Vitreous (PHPV) LIV Edward Jackson Memorial Lecture (Q41645582) (← links)
• Identification of a Recurrent Missense Mutation in the Norrie Disease Gene Associated with a Simplex Case of Exudative Vitreoretinopathy (Q48000151) (← links)
• Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal Norrin. (Q50512238) (← links)
• Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease gene (Q51006076) (← links)
• History of retina 1896-1996. (Q53619901) (← links)
• Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy (Q70821102) (← links)
• Familial exudative vitreoretinopathy: further evidence for genetic heterogeneity (Q73123845) (← links)
• Linkage and candidate gene analysis of autosomal-dominant familial exudative vitreoretinopathy (Q73184250) (← links)
• Evidence for Genetic Heterogeneity in X-Linked Familial Exudative Vitreoretinopathy (Q73702596) (← links)
• Vitrectomy for rhegmatogenous or tractional retinal detachment with familial exudative vitreoretinopathy (Q77872878) (← links)
• Cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy (Q79167896) (← links)
• Wnt Signaling in vascular eye diseases (Q90249957) (← links)