Pages that link to "Q77372768"
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The following pages link to Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers (Q77372768):
Displaying 3 items.
- Early diagnosis of Usher syndrome in children (Q24536663) (← links)
- Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing (Q34166178) (← links)
- A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services. (Q34862383) (← links)