Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

Author:

Doucette Lance,Merner Nancy D,Cooke Sandra,Ives Elizabeth,Galutira Dante,Walsh Vanessa,Walsh Tom,MacLaren Linda,Cater Tracey,Fernandez Bridget,Green Jane S,Wilcox Edward R,Shotland Larry,Li X C,Lee Ming,King Mary-Claire,Young Terry-Lynn

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference49 articles.

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3. Martin LJ, Crawford MH, Koertvelyessy T, Keeping D, Collins M, Huntsman R : The population structure of ten Newfoundland outports. Hum Biol 2000; 72: 997–1016.

4. Bear JC, Nemec TF, Kennedy JC et al: Persistent genetic isolation in outport Newfoundland. Am J Med Genet 1987; 27: 807–830.

5. Bear JC, Nemec TF, Kennedy JC et al: Inbreeding in outport Newfoundland. Am J Med Genet 1988; 29: 649–660.

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