Development of a genotyping microarray for Usher syndrome
Cremers, Frans P M, Kimberling, William J, Külm, Maigi, de Brouwer, Arjan P, van Wijk, Erwin, te Brinke, Heleen, Cremers, Cor W R J, Hoefsloot, Lies H, Banfi, Sandro, Simonelli, Francesca, Fleischhauer, Johannes C, Berger, Wolfgang, Kelley, Phil M, Haralambous, Elene, Bitner-Glindzicz, Maria, Webster, Andrew R, Saihan, Zubin, De Baere, Elfride, Leroy, Bart P, Silvestri, Giuliana, McKay, Gareth J, Koenekoop, Robert K, Millan, Jose M, Rosenberg, Thomas, Joensuu, Tarja, Sankila, Eeva-Marja, Weil, Dominique, Weston, Mike D, Wissinger, Bernd, Kremer, Hannie
Published in Journal of medical genetics (01.02.2007)
Published in Journal of medical genetics (01.02.2007)
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Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations
USAMI, S.-I, ABE, S, WESTON, M. D, SHINKAWA, H, VAN CAMP, G, KIMBERLING, W. J
Published in Human genetics (01.02.1999)
Published in Human genetics (01.02.1999)
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Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation
Abe, S, Usami, S, Shinkawa, H, Weston, M D, Overbeck, L D, Hoover, D M, Kenyon, J B, Horai, S, Kimberling, W J
Published in European journal of human genetics : EJHG (01.11.1998)
Published in European journal of human genetics : EJHG (01.11.1998)
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The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A)
Kelley, Philip M., Weston, Mike D., Chen, Zheng-Yi, Orten, Dana J., Hasson, Tama, Overbeck, Larry D., Pinnt, Jeff, Talmadge, Catherine B., Ing, Paul, Mooseker, Mark S., Corey, David, Sumegi, Janos, Kimberling, William J.
Published in Genomics (San Diego, Calif.) (15.02.1997)
Published in Genomics (San Diego, Calif.) (15.02.1997)
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