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Plos One
|
October 17, 2013
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS
Maiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, et al.
Journal of Human Genetics
|
January 22, 2016
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing
Hidekane Yoshimura, Maiko Miyagawa, Kozo Kumakawa, et al.
Genetic Testing and Molecular Biomarkers
|
December 29, 2020
Improvement of a Rapid and Highly Sensitive Method for the Diagnosis of the Mitochondrial m.1555A>G Mutation Based on a Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip
Yuichi Isaka, Shin-Ya Nishio, Eiji Hishinuma, et al.
Anatomical Record (Hoboken, N.J. : 2007)
|
February 7, 2020
Cochlear Implantation From the Perspective of Genetic Background
Shin-Ichi Usami, Shin-Ya Nishio, Hideaki Moteki, et al.
Genes
|
March 4, 2020
Haplotype Analysis of <i>GJB2</i> Mutations: Founder Effect or Mutational Hot Spot?
Jun Shinagawa, Hideaki Moteki, Shin-Ya Nishio, et al.
Acta Oto-Laryngologica
|
April 21, 2023
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation
Jun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, et al.
Journal of Bacteriology
|
January 24, 2006
Anatomy of the replication origin of plasmid ColE2-P9
Masaru Yagura, Shin-Ya Nishio, Hideki Kurozumi, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 18, 2015
Germinal mosaicism in a family with BO syndrome
Maiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 20, 2015
Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance
Aya Ichinose, Hideaki Moteki, Mitsuru Hattori, et al.
Acta Oto-Laryngologica
|
May 27, 2011
Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord
Sakiko Furutate, Satoshi Iwasaki, Shin-ya Nishio, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 142) with videos related to
Sort By:
Page
of 15
Plos One
|
October 17, 2013
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS
Maiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, et al.
Journal of Human Genetics
|
January 22, 2016
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing
Hidekane Yoshimura, Maiko Miyagawa, Kozo Kumakawa, et al.
Genetic Testing and Molecular Biomarkers
|
December 29, 2020
Improvement of a Rapid and Highly Sensitive Method for the Diagnosis of the Mitochondrial m.1555A>G Mutation Based on a Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip
Yuichi Isaka, Shin-Ya Nishio, Eiji Hishinuma, et al.
Anatomical Record (Hoboken, N.J. : 2007)
|
February 7, 2020
Cochlear Implantation From the Perspective of Genetic Background
Shin-Ichi Usami, Shin-Ya Nishio, Hideaki Moteki, et al.
Genes
|
March 4, 2020
Haplotype Analysis of <i>GJB2</i> Mutations: Founder Effect or Mutational Hot Spot?
Jun Shinagawa, Hideaki Moteki, Shin-Ya Nishio, et al.
Acta Oto-Laryngologica
|
April 21, 2023
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation
Jun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, et al.
Journal of Bacteriology
|
January 24, 2006
Anatomy of the replication origin of plasmid ColE2-P9
Masaru Yagura, Shin-Ya Nishio, Hideki Kurozumi, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 18, 2015
Germinal mosaicism in a family with BO syndrome
Maiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 20, 2015
Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance
Aya Ichinose, Hideaki Moteki, Mitsuru Hattori, et al.
Acta Oto-Laryngologica
|
May 27, 2011
Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord
Sakiko Furutate, Satoshi Iwasaki, Shin-ya Nishio, et al.
Page
of 15