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Showing results 6 to 11 of 11< previous 
Issue DateTitleAuthor(s)
2023-08-02Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.Freeman, L; Bristowe, L; Kirk, EP; Delatycki, MB; Scully, JL
2022-11-01The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and ImplementationArchibald, AD; McClaren, BJ; Caruana, J; Tutty, E; King, EA; Halliday, JL; Best, S; Kanga-Parabia, A; Bennetts, BH; Cliffe, CC; Madelli, EO; Ho, G; Liebelt, J; Long, JC; Braithwaite, J; Kennedy, J; Massie, J; Emery, JD; McGaughran, J; Marum, JE; Boggs, K; Barlow-Stewart, K; Burnett, L; Dive, L; Freeman, L; Davis, MR; Downes, MJ; Wallis, M; Ferrie, MM; Pachter, N; Scuffham, PA; Casella, R; Allcock, RJN; Ong, R; Edwards, S; Righetti, S; Lunke, S; Lewis, S; Walker, SP; Boughtwood, TF; Hardy, T; Newson, AJ; Kirk, EP; Laing, NG; Delatycki, MB
2022-09The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review.Freeman, L; Righetti, S; Delatycki, MB; Scully, JL; Kirk, EP
2023-05Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening.Freeman, L; Delatycki, MB; Scully, JL; Briggs, N; Kirk, EP
2022-12Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss.Freeman, L; Delatycki, MB; Leach Scully, J; Kirk, EP
2018-12-01Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disordersEwans, LJ; Schofield, D; Shrestha, R; Zhu, Y; Gayevskiy, V; Ying, K; Walsh, C; Lee, E; Kirk, EP; Colley, A; Ellaway, C; Turner, A; Mowat, D; Worgan, L; Freckmann, ML; Lipke, M; Sachdev, R; Miller, D; Field, M; Dinger, ME; Buckley, MF; Cowley, MJ; Roscioli, T
Showing results 6 to 11 of 11< previous