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Publications by Terry-Lynn Young

A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31

American Journal of Human Genetics

English

Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15

European Journal of Human Genetics

English