Last Posted: Apr 04, 2019
- Diagnosis, Intervention, and Prevention of Genetic Hearing Loss.
Yang Tao et al. Advances in experimental medicine and biology 2019 113073-92 - ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.
DiStefano Marina T et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Mar - Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.
Sun Yan et al. Medicine 2019 Mar 98(12) e14860 - Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.
Wang Qiuju et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Mar - Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.
Liu Yanhui et al. International journal of pediatric otorhinolaryngology 2019 Feb 11782-87 - Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.
Lu Chun-Yi et al. The Journal of pediatrics 2018 199144-150.e1 - Treatment and long-term outcome in primary distal renal tubular acidosis.
Lopez-Garcia Sergio Camilo et al. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2019 Feb - Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan.
Liu Wei-Hsiu et al. PloS one 2019 14(1) e0211261 - [The clinical application of gene diagnosis and genetic counseling on hereditary hearing loss].
Zhang Z K et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2019 Jan 33(1) 58-62 - Hereditary hearing loss; about the known and the unknown.
Kremer Hannie et al. Hearing research 2019 Jan
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