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Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
Downie L, Halliday J, Burt R, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter MF, Saunders K, Rose E, Lewis S, Jarmolowicz A, Phelan D, Rehm HL; Melbourne Genomics Health Alliance; Amor DJ. Downie L, et al. Among authors: rose e. Eur J Hum Genet. 2020 May;28(5):587-596. doi: 10.1038/s41431-019-0553-8. Epub 2019 Dec 12. Eur J Hum Genet. 2020. PMID: 31827275 Free PMC article.
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
Downie L, Halliday J, Burt R, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter MF, Saunders K, Rose E, Lewis S, Jarmolowicz A, Phelan D, Rehm HL; Melbourne Genomics Health Alliance; Amor DJ. Downie L, et al. Among authors: rose e. Eur J Hum Genet. 2021 Feb;29(2):363. doi: 10.1038/s41431-020-00750-4. Eur J Hum Genet. 2021. PMID: 33168987 Free PMC article. No abstract available.
Childhood Hearing Australasian Medical Professionals network: Consensus guidelines on investigation and clinical management of childhood hearing loss.
Sung V, Downie L, Paxton GA, Liddle K, Birman CS, Chan WW, Cottier C, Harris A, Hunter M, Peadon E, Peacock K, Roddick L, Rose E, Saunders K, Amor DJ. Sung V, et al. Among authors: rose e. J Paediatr Child Health. 2019 Sep;55(9):1013-1022. doi: 10.1111/jpc.14508. J Paediatr Child Health. 2019. PMID: 31524978 No abstract available.
Response to E Satter and B Lohse.
Keller KL, Pearce AL, Fuchs B, Rolls BJ, Wilson SJ, Geier CF, Rose E, Garavan H. Keller KL, et al. Among authors: rose e. J Nutr. 2024 Dec;154(12):3854-3855. doi: 10.1016/j.tjnut.2024.10.003. J Nutr. 2024. PMID: 39638450 No abstract available.
1,218 results