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BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
Acta Oto-Laryngologica|September 14, 2007
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutationsHiroaki Suzuki, Aki Oshima, Koji Tsukamoto, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's diseaseShin-ichi Usami, Kentaro Takahashi, Isamu Yuge, et al.
Breast Cancer (Tokyo, Japan)|September 23, 2008
MR-guided vacuum-assisted breast biopsy: is it an essential technique?Mitsuhiro Tozaki, Norie Yamashiro, Takako Suzuki, et al.
Journal of Human Genetics|February 9, 2005
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patternsTomohiro Oguchi, Akihiro Ohtsuka, Shigenari Hashimoto, et al.
Breast Cancer (Tokyo, Japan)|February 28, 2008
New preoperative MRI marking technique for a patient with ductal carcinoma in situTomoko Ogawa, Mitsuhiro Tozaki, Norie Yamashiro, et al.
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