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Publications by X C Li
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
Genetics
The Pachytene Checkpoint and Its Relationship to Evolutionary Patterns of Polyploidization and Hybrid Sterility
Heredity
Genetics