Newborn hearing concurrent genetic screening for hearing impairment—A clinical practice in 58,397 neonates in Tianjin, China

Chelex 100 as a Medium for Simple Extraction of DNA for PCR-Based Typing from Forensic Material

P. Sean Walsh, David A. Metzger, Russell Higuchi · BioTechniques · 2013 · 5.9K citations · Full text

Medicine, Molecular Biology, Molecular Genetics +14

Language of Early- and Later-identified Children With Hearing Loss

Christine Yoshinaga‐Itano, Allison L. Sedey, Diane K. Coulter et al. · PEDIATRICS · 1998 · 2.1K citations

Education, Audiology, Special Education +17

Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss

Philip M. Kelley, David J. Harris, B.C. Comer et al. · The American Journal of Human Genetics · 1998 · 506 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment studyCommentary: Universal newborn hearing screening: implications for coordinating and developing services for deaf and hearing impaired children

Heather Fortnum, A. Quentin Summerfield, Sally Hind · BMJ · 2001 · 493 citations · Full text

Medicine, Audiology, Pediatrics +17

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 426 citations

Life Sciences, Genetics, Molecular Genetics +14