Last Posted: Mar 20, 2020
- Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach
BJ Kim et al, Genetics in Medicine, March 17, 2020 - Establishing Genotype-phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and Rehabilitation.
Molina-Ramírez Leslie P et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 Apr 41(4) 431-437 - Genetic testing has the potential to impact hearing preservation following cochlear implantation.
Yoshimura Hidekane et al. Acta oto-laryngologica 2020 Mar 1-7 - [Clinical practice guidelines for hereditary non-syndromic deafness].
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Mar 37(3) 269-276 - Expanded carrier screening for preconception reproductive risk assessment: Prevalence of carrier status in a Mexican population.
Hernandez-Nieto Carlos et al. Prenatal diagnosis 2020 Jan - Application of Big Data to Support Evidence-Based Public Health Policy Decision-Making for Hearing.
Saunders Gabrielle H et al. Ear and hearing 2020 Jan - UK Newborn Trial to Assess PCR Test for Antibiotic-Induced Hearing Loss
GenomeWeb, Jan 27, 2020. - Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection.
Dobbins G Clement et al. BMC infectious diseases 2019 Dec (1) 1046 - Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period.
Bazazzadegan Niloofar et al. Iranian journal of public health 2019 Oct 48(10) 1910-1915 - Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
Downie Lilian et al. European journal of human genetics : EJHG 2019 Dec
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