Last Posted: Dec 13, 2019
- 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 - Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels.
Kanavy Dona M et al. Genome medicine 2019 Nov 11(1) 77 - Alport Syndrome in Women and Girls.
Savige Judy et al. Clinical journal of the American Society of Nephrology : CJASN 2016 11(9) 1713-20 - Clinical utility of next-generation sequencing in the aetiological diagnosis of sensorineural hearing loss in a Childhood Hearing Loss Unit.
Costales María et al. Acta otorrinolaringologica espanola 2019 Nov - Fulfilling the Promise - Ensuring the Success of Newborn Screening throughout Life
CDC, November 2019 - Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review.
Koohiyan Mahbobeh et al. International journal of pediatric otorhinolaryngology 2019 Oct 129109756 - NIH Director Backs Moratorium for Heritable Genome Editing
Gen News, November 8, 2019 - Genetic therapies for hearing loss: Accomplishments and remaining challenges.
Taiber Shahar et al. Neuroscience letters 2019 Oct 134527 - Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.
Dai Pu et al. American journal of human genetics 2019 Sep - Increase in Developmental Disabilities Among Children in the United States
CDC, September 2019
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