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Hendee K 1
Showing records 1 to 1 | Display all abstracts from Hendee K73485 Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial and other systemic features in a three generation human pedigree
Hendee K; Wang LW; Reis LM; Rice GM; Apte SS; Semina EV
Human Mutation 2017; 38: 1485-1490
