Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  17 results for ""Deafness""

Your Filters

Publication : international journal of pediatric otorhinolaryngology Language : english Subject : genetic testing
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Suspension array-based deafness genetic screening in 53,033 Chinese newborns identifies high prevalence of 109 G>A in GJB2.

  • Authors : Zou Y; Department of Otolaryngology, Guangdong Women and Children Hospital, Guangzhou, 511400, China.; Dai QQ

Subjects: Genetic Testing* ; Mutation* ; Neonatal Screening*

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Nov; Vol. 126, pp. 109630. Date of Electronic Publication: Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Combined hearing screening and genetic screening of deafness among Hakka newborns in China.

  • Authors : Zeng X; Laboratory of Medical Genetics, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China; Department of Clinical Laboratory, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China. Electronic address: .

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis ; Hearing Tests/Hearing Tests/Hearing Tests/*methods

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2020 Sep; Vol. 136, pp. 110120. Date of Electronic Publication: Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials.

  • Authors : Chen S; Health Care Dept, Guangdong Women and Children's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.; Liang Z

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*statistics & numerical data; Asian People/Asian People/Asian People/genetics

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Jun; Vol. 121, pp. 99-108. Date of Electronic Publication: Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.

  • Authors : Liu Y; Department of Prenatal Diagnosis Center, Dongguan Maternal and Child Health Hospital, Dongguan 523112, Guangdong, China.; Ye L

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Tests/Hearing Tests/Hearing Tests/*methods

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Feb; Vol. 117, pp. 82-87. Date of Electronic Publication: Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

  • Authors : Han B; Department of Otolaryngology-Head and Neck Surgery, and Institute of Otolaryngology, Chinese People's Liberation Army General Hospital, Beijing, China.; Zong L

Subjects: Genetic Predisposition to Disease*; Anion Transport Proteins/Anion Transport Proteins/Anion Transport Proteins/*genetics ; Connexins/Connexins/Connexins/*genetics

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2013 Sep; Vol. 77 (9), pp. 1440-5. Date of Electronic Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese children.

  • Authors : Hayashi C; Department of Otorhinolaryngology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan. ; Funayama M

Subjects: Point Mutation*; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*epidemiology

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2011 Feb; Vol. 75 (2), pp. 211-4. Date of Electronic Publication:Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Parental attitudes toward genetic testing for prelingual deafness in China.

  • Authors : Fu S; Department of Medical Genetics, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.; Dong J

Subjects: Genetic Testing*/Genetic Testing*/Genetic Testing*/psychology ; Health Knowledge, Attitudes, Practice*; Deafness/Deafness/Deafness/*diagnosis

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2010 Oct; Vol. 74 (10), pp. 1122-5. Date of Electronic Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Auditory screening concurrent deafness predisposing genes screening in 10,043 neonates in Gansu province, China.

  • Authors : Zhang Z; School of Basic Medical Sciences, Lanzhou University, Lanzhou, China.; Ding W

Subjects: Genetic Testing* ; Neonatal Screening*; Deafness/Deafness/Deafness/*diagnosis

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2012 Jul; Vol. 76 (7), pp. 984-8. Date of Electronic Publication:Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Minimally invasive genetic screen for GJB2 related deafness using dried blood spots.

  • Authors : Nagy AL; University of Szeged, Albert Szent-Györgyi Pharmaceutical and Medical Centre, Department of Oto-rhino-laryngology and Head and Neck Surgery, 6725, Tisza Lajos krt. 111, Szeged, Hungary. ; Csáki R

Subjects: Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*blood ; Deafness/Deafness/Deafness/*genetics

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2010 Jan; Vol. 74 (1), pp. 75-81. Date of Electronic Publication:Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

  • Authors : Tamayo ML; Instituto de Genética Humana, Universidad Javeriana, Bogotá, Colombia. ; Olarte M

Subjects: Genetic Testing*; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*epidemiology

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2009 Jan; Vol. 73 (1), pp. 97-101. Date of Electronic Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Print

Record details

Read More Add to Saved list
×
  • 1-10 of  17 results for ""Deafness""