| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Deafness Gene Variations in a 1120 Nonsyndromic Hearing Loss Cohort
|
Nishio, Shin-ya
|
|
2015
|
124 |
1_suppl |
p. 49S-60S
|
artikel
|
| 2 |
De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss
|
Moteki, Hideaki
|
|
2015
|
124 |
1_suppl |
p. 169S-176S
|
artikel
|
| 3 |
Detailed Hearing and Vestibular Profiles in the Patients with COCH Mutations
|
Tsukada, Keita
|
|
2015
|
124 |
1_suppl |
p. 100S-110S
|
artikel
|
| 4 |
Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations
|
Tsukada, Keita
|
|
2015
|
124 |
1_suppl |
p. 61S-76S
|
artikel
|
| 5 |
Gene Expression Profiles of the Cochlea and Vestibular Endorgans
|
Nishio, Shin-ya
|
|
2015
|
124 |
1_suppl |
p. 6S-48S
|
artikel
|
| 6 |
Germinal Mosaicism in a Family With BO Syndrome
|
Miyagawa, Maiko
|
|
2015
|
124 |
1_suppl |
p. 118S-122S
|
artikel
|
| 7 |
Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation
|
Moteki, Hideaki
|
|
2015
|
124 |
1_suppl |
p. 177S-183S
|
artikel
|
| 8 |
Identification of a Novel CLRN1 Gene Mutation in Usher Syndrome Type 3
|
Yoshimura, Hidekane
|
|
2015
|
124 |
1_suppl |
p. 94S-99S
|
artikel
|
| 9 |
Massively Parallel DNA Sequencing Successfully Identified Seven Families With Deafness-Associated MYO6 Mutations
|
Miyagawa, Maiko
|
|
2015
|
124 |
1_suppl |
p. 148S-157S
|
artikel
|
| 10 |
Molecular Diagnosis of Deafness—A Preface
|
Usami, Shin-ichi
|
|
2015
|
124 |
1_suppl |
p. 5S
|
artikel
|
| 11 |
Mutational Spectrum and Clinical Features of Patients With ACTG1 Mutations Identified by Massively Parallel DNA Sequencing
|
Miyagawa, Maiko
|
|
2015
|
124 |
1_suppl |
p. 84S-93S
|
artikel
|
| 12 |
Mutations in LOXHD1 Gene Cause Various Types and Severities of Hearing Loss
|
Mori, Kentaro
|
|
2015
|
124 |
1_suppl |
p. 135S-141S
|
artikel
|
| 13 |
Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing Loss
|
Miyagawa, Maiko
|
|
2015
|
124 |
1_suppl |
p. 158S-168S
|
artikel
|
| 14 |
Non-ocular Stickler Syndrome With a Novel Mutation in COL11A2 Diagnosed by Massively Parallel Sequencing in Japanese Hearing Loss Patients
|
Iwasa, Yoh-ichiro
|
|
2015
|
124 |
1_suppl |
p. 111S-117S
|
artikel
|
| 15 |
Novel ABHD12 Mutations in PHARC Patients
|
Yoshimura, Hidekane
|
|
2015
|
124 |
1_suppl |
p. 77S-83S
|
artikel
|
| 16 |
Novel Mutations in GRXCR1 at DFNB25 Lead to Progressive Hearing Loss and Dizziness
|
Mori, Kentaro
|
|
2015
|
124 |
1_suppl |
p. 129S-134S
|
artikel
|
| 17 |
Novel Mutations in LRTOMT Associated With Moderate Progressive Hearing Loss in Autosomal Recessive Inheritance
|
Ichinose, Aya
|
|
2015
|
124 |
1_suppl |
p. 142S-147S
|
artikel
|
| 18 |
Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss
|
Sakuma, Naoko
|
|
2015
|
124 |
1_suppl |
p. 184S-192S
|
artikel
|
| 19 |
The Patients Associated With TMPRSS3 Mutations Are Good Candidates for Electric Acoustic Stimulation
|
Miyagawa, Maiko
|
|
2015
|
124 |
1_suppl |
p. 193S-204S
|
artikel
|
| 20 |
USH2 Caused by GPR98 Mutation Diagnosed by Massively Parallel Sequencing in Advance of the Occurrence of Visual Symptoms
|
Moteki, Hideaki
|
|
2015
|
124 |
1_suppl |
p. 123S-128S
|
artikel
|
Tijdschrift beschrijving