Pages that link to "Q34461621"

The following pages link to Linkage analysis of two families with X-linked recessive congenital motor nystagmus (Q34461621):

Displaying 9 items.

• CSNB1 in Chinese families associated with novel mutations in NYX (Q28238064) (← links)
• CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes (Q34329072) (← links)
• A review of the molecular genetics of congenital Idiopathic Nystagmus (CIN). (Q34730771) (← links)
• A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family. (Q36496262) (← links)
• Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus. (Q36691929) (← links)
• Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism. (Q36957638) (← links)
• Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation. (Q51752663) (← links)
• Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1. (Q51796225) (← links)
• Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1 (Q79919265) (← links)