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Year Number of Results
2011 1
2012 2
2013 2
2014 3
2018 2
2020 1
2022 1
2023 2
2024 1

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Page 1
Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.
Farrar MA, Kariyawasam D, Grattan S, Bayley K, Davis M, Holland S, Waddel LB, Jones K, Lorentzos M, Ravine A, Wotton T, Wiley V; DMD NBS Working Group. Farrar MA, et al. Among authors: wotton t. J Neuromuscul Dis. 2023;10(1):15-28. doi: 10.3233/JND-221535. J Neuromuscul Dis. 2023. PMID: 36373292 Free PMC article. Review.
The evolution of blood-spot newborn screening.
Bhattacharya K, Wotton T, Wiley V. Bhattacharya K, et al. Among authors: wotton t. Transl Pediatr. 2014 Apr;3(2):63-70. doi: 10.3978/j.issn.2224-4336.2014.03.08. Transl Pediatr. 2014. PMID: 26835325 Free PMC article. Review.
Fragile X protein in newborn dried blood spots.
Adayev T, LaFauci G, Dobkin C, Caggana M, Wiley V, Field M, Wotton T, Kascsak R, Nolin SL, Glicksman A, Hosmer N, Brown WT. Adayev T, et al. Among authors: wotton t. BMC Med Genet. 2014 Oct 28;15:119. doi: 10.1186/s12881-014-0119-0. BMC Med Genet. 2014. PMID: 25348928 Free PMC article.
Maternal attitudes to newborn screening for fragile X syndrome.
Christie L, Wotton T, Bennetts B, Wiley V, Wilcken B, Rogers C, Boyle J, Turner C, Hansen J, Hunter M, Goel H, Field M. Christie L, et al. Among authors: wotton t. Am J Med Genet A. 2013 Feb;161A(2):301-11. doi: 10.1002/ajmg.a.35752. Epub 2013 Jan 9. Am J Med Genet A. 2013. PMID: 23303663
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts.
Kraan CM, Bui QM, Field M, Archibald AD, Metcalfe SA, Christie LM, Bennetts BH, Oertel R, Smith MJ, du Sart D, Bruno D, Wotton TL, Amor DJ, Francis D, Godler DE. Kraan CM, et al. Among authors: wotton tl. Genet Med. 2018 Dec;20(12):1627-1634. doi: 10.1038/gim.2018.52. Epub 2018 Mar 29. Genet Med. 2018. PMID: 29595813 Free article.
13 results