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NARA Subscribed4
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Springer Nature4
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Human Genetics3
Mammalian Genome1
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20202
20161
19971
Kathy Frees results 4 · Newest (Page 1/1, per page 25)
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Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossNARA Subscribed
Human Genetics · 2020 · Vol. 139 · Issue 12 · Springer
Kevin T. Booth; Amama Ghaffar; Muhammad Rashid; Luke T. Hovey; Mureed Hussain; Kathy Frees; Erika M. Renkes; Carla J. Nishimura; Mohsin Shahzad; Richard J. Smith; Zubair Ahmed; Hela Azaiez; Saima Riazuddin
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A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populationsNARA Subscribed
Human Genetics · 2020 · Vol. 139 · Issue 10 · Springer
W. Daniel Walls; Hideaki Moteki; Taylor R. Thomas; Shin-ya Nishio; Hidekane Yoshimura; Yoichiro Iwasa; Kathy L. Frees; Carla J. Nishimura; Hela Azaiez; Kevin T. Booth; Robert J. Marini; Diana L. Kolbe; A. Monique Weaver; Amanda M. Schaefer; Kai Wang; Terry A. Braun; Shin-ichi Usami; Peter G. Barr-Gillespie; Guy P. Richardson; Richard J. Smith; Thomas L. Casavant
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Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing lossNARA Subscribed
Human Genetics · 2016 · Vol. 135 · Issue 4 · Springer
Christina M. Sloan-Heggen; Amanda O. Bierer; A. Eliot Shearer; Diana L. Kolbe; Carla J. Nishimura; Kathy L. Frees; Sean S. Ephraim; Seiji B. Shibata; Kevin T. Booth; Colleen A. Campbell; Paul T. Ranum; Amy E. Weaver; E. Ann Black-Ziegelbein; Donghong Wang; Hela Azaiez; Richard J. H. Smith
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Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locusNARA Subscribed
Mammalian Genome · 1997 · Vol. 8 · Issue 10 · Springer
Stacia Peiffer-Schneider; Brian C. Schutte; Jeffrey C. Murray; Kathy L. Frees; Kimberly Williamson; Nancy J. Leysens; David A. Schwartz
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