Pages that link to "Q50762610"

The following pages link to Autosomal dominant keratoconus as the chief ocular symptom in Lobstein osteogenesis imperfecta tarda (Q50762610):

Displaying 17 items.

• Corneal cross-linking treatment of keratoconus (Q26775836) (← links)
• Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus. (Q34229424) (← links)
• Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32. (Q34881029) (← links)
• Gene therapy in keratoconus (Q35098491) (← links)
• Bilateral papilledema in a child with osteogenesis imperfecta (Q37343147) (← links)
• Molecular and Histopathological Changes Associated with Keratoconus. (Q37637768) (← links)
• The Genetics of Keratoconus: A Review (Q38116511) (← links)
• Epidemiological aspects of keratoconus in children (Q45129118) (← links)
• Osteogenesis imperfecta and keratoconus in an Italian family (Q50151323) (← links)
• Osteogenesis imperfecta and glaucoma. A case report (Q50264334) (← links)
• Variants in SKP1, PROB1, and IL17B genes at keratoconus 5q31.1-q35.3 susceptibility locus identified by whole-exome sequencing (Q51431421) (← links)
• Keratoglobus lesions in the eyes of rearing broiler breeders (Q51702172) (← links)
• Keratoconus (Q54158058) (← links)
• The genetics of keratoconus (Q60518088) (← links)
• Genetic Aspects of Keratoconus: A Literature Review Exploring Potential Genetic Contributions and Possible Genetic Relationships with Comorbidities. (Q64987781) (← links)
• Familial association of keratoconus and granular corneal dystrophy: The familial case series (Q91814625) (← links)
• PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus (Q92096708) (← links)