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Page 1
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
Genet Med. 2022 Jan;24(1):130-145. doi: 10.1016/j.gim.2021.09.001. Epub 2021 Nov 30.
Genet Med. 2022.
PMID: 34906502
Free article.
Clinically Responsive Genomic Analysis Pipelines: Elements to Improve Detection Rate and Efficiency.
Sundercombe SL, Berbic M, Evans CA, Cliffe C, Elakis G, Temple SEL, Selvanathan A, Ewans L, Quayum N, Nixon CY, Dias KR, Lang S, Richards A, Goh S, Wilson M, Mowat D, Sachdev R, Sandaradura S, Walsh M, Farrar MA, Walsh R, Fletcher J, Kirk EP, Teunisse GM, Schofield D, Buckley MF, Zhu Y, Roscioli T.
Sundercombe SL, et al.
J Mol Diagn. 2021 Jul;23(7):894-905. doi: 10.1016/j.jmoldx.2021.04.007. Epub 2021 May 5.
J Mol Diagn. 2021.
PMID: 33962052
Free article.
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Concurrent maternal malignancy and fetal trisomy detected using genome-wide noninvasive prenatal screening.
Scott F, Smet ME, Hardy T, Sundercombe S, Friedlander M, Carey L, Kirk E, Li B, McLennan A.
Scott F, et al. Among authors: sundercombe s.
Prenat Diagn. 2021 Sep;41(10):1273-1276. doi: 10.1002/pd.6020. Epub 2021 Aug 14.
Prenat Diagn. 2021.
PMID: 34318961
No abstract available.
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Audit of a clinical guideline for neonatal hypoglycaemia screening.
Sundercombe SL, Raynes-Greenow CH, Carberry AE, Turner RM, Jeffery HE.
Sundercombe SL, et al.
J Paediatr Child Health. 2013 Oct;49(10):833-8. doi: 10.1111/jpc.12293. Epub 2013 Jun 24.
J Paediatr Child Health. 2013.
PMID: 23795770
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Do neonatal hypoglycaemia guidelines in Australia and New Zealand facilitate breast feeding?
Sundercombe SL, Raynes-Greenow CH, Turner RM, Jeffery HE.
Sundercombe SL, et al.
Midwifery. 2014 Dec;30(12):1179-86. doi: 10.1016/j.midw.2014.04.004. Epub 2014 Apr 28.
Midwifery. 2014.
PMID: 24835006
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