Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Concurrent maternal malignancy and fetal trisomy detected using genome-wide noninvasive prenatal screening.
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.
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.
Item in Clipboard
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
Bournazos AM, Riley LG, Bommireddipalli S, Ades L, Akesson LS, Al-Shinnag M, Alexander SI, Archibald AD, Balasubramaniam S, Berman Y, Beshay V, Boggs K, Bojadzieva J, Brown NJ, Bryen SJ, Buckley MF, Chong B, Davis MR, Dawes R, Delatycki M, Donaldson L, Downie L, Edwards C, Edwards M, Engel A, Ewans LJ, Faiz F, Fennell A, Field M, Freckmann ML, Gallacher L, Gear R, Goel H, Goh S, Goodwin L, Hanna B, Harraway J, Higgins M, Ho G, Hopper BK, Horton AE, Hunter MF, Huq AJ, Josephi-Taylor S, Joshi H, Kirk E, Krzesinski E, Kumar KR, Lemckert F, Leventer RJ, Lindsey-Temple SE, Lunke S, Ma A, Macaskill S, Mallawaarachchi A, Marty M, Marum JE, McCarthy HJ, Menezes MP, McLean A, Milnes D, Mohammad S, Mowat D, Niaz A, Palmer EE, Patel C, Patel SG, Phelan D, Pinner JR, Rajagopalan S, Regan M, Rodgers J, Rodrigues M, Roxburgh RH, Sachdev R, Roscioli T, Samarasekera R, Sandaradura SA, Savva E, Schindler T, Shah M, Sinnerbrink IB, Smith JM, Smith RJ, Springer A, Stark Z, Strom SP, Sue CM, Tan K, Tan TY, Tantsis E, Tchan MC, Thompson BA, Trainer AH, van Spaendonck-Zwarts K, Walsh R, Warwick L, White S, White SM, Williams MG, Wilson MJ, Wong WK, Wright DC, Yap P, Yeung A, Young H, Jones KJ, Bennetts…
See abstract for full author list ➔
Bournazos AM, et al.
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.
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
Cite
Cite