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Prenatal features of Noonan syndrome.
Nisbet DL, Griffin DR, Chitty LS. Nisbet DL, et al. Prenat Diagn. 1999 Jul;19(7):642-7. doi: 10.1002/(sici)1097-0223(199907)19:7<642::aid-pd610>3.0.co;2-1. Prenat Diagn. 1999. PMID: 10419612
Right-sided aortic arch in the age of microarray.
O'Mahony EF, Hutchinson DP, McGillivray G, Nisbet DL, Palma-Dias R. O'Mahony EF, et al. Among authors: nisbet dl. Prenat Diagn. 2017 May;37(5):440-445. doi: 10.1002/pd.5029. Epub 2017 Mar 12. Prenat Diagn. 2017. PMID: 28207948
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.
Kluckow E, Halliday J, Poulton A, Lindquist A, Hutchinson B, Bethune M, Bonacquisto L, Da Silva Costa F, Gugasyan L, Harraway J, Howden A, Kulkarni A, Martin N, McCoy R, Menezes M, Nisbet D, Palma-Dias R, Pertile MD, Poulakis Z, Hui L. Kluckow E, et al. Prenat Diagn. 2019 Dec;39(13):1254-1261. doi: 10.1002/pd.5577. Epub 2019 Nov 6. Prenat Diagn. 2019. PMID: 31691307
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Hui L, Poulton A, Kluckow E, Lindquist A, Hutchinson B, Pertile MD, Bonacquisto L, Gugasyan L, Kulkarni A, Harraway J, Howden A, McCoy R, Costa FDS, Menezes M, Palma-Dias R, Nisbet D, Martin N, Bethune M, Poulakis Z, Halliday J. Hui L, et al. Hum Reprod. 2020 Mar 27;35(3):694-704. doi: 10.1093/humrep/dez286. Hum Reprod. 2020. PMID: 32207823
21 results