Search Results

Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients.

• Authors : Miyagawa, Maiko; Naito, Takehiko; Nishio, Shin-ya

Subjects: DEAFNESS; EXONS (Genetics); NUCLEOTIDE sequence

• Source: PLoS ONE; Aug2013, Vol. 8 Issue 8, p1-11, 11p

Record details

Outcomes of cochlear implantation for the patients with specific genetic etiologies: a systematic literature review.

• Authors : Nishio, Shin-ya (AUTHOR); Usami, Shin-ichi (AUTHOR)

Subjects: GENETIC disorder diagnosis; COCHLEAR implants; TREATMENT effectiveness

• Source: Acta Oto-Laryngologica. Jul2017, Vol. 137 Issue 7, p730-742. 14p.

Record details

GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon.

• Authors : Trotta, Luca (AUTHOR); Iacona, Elisabetta (AUTHOR); Primignani, Paola (AUTHOR)

Subjects: HEARING impaired children; COMPUTER software; HEARING disordersSUB-Saharan Africa; CAMEROON

• Source: International Journal of Audiology. Feb2011, Vol. 50 Issue 2, p133-138. 6p. 4 Charts.

Record details

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

• Authors : Green, Glenn E.; Scott, Daryl A.; McDonald, Joshua M.

Subjects: GENETICS of deafness; GENETICS; GENETIC engineering

• Source: JAMA: Journal of the American Medical Association; 6/16/99, Vol. 281 Issue 23, p2211-2216, 6p, 3 Charts

Record details

Salem Health: Genetics and Inherited Conditions

• Authors : Jeffrey A. Knight, Ph.D

Subjects: Genetics; Genetic disordersMEDICAL / Genetics; HEALTH & FITNESS / Diseases & Conditions / Genetic

Record details