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Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy.
Prenat Diagn. 2022 May;42(6):762-774. doi: 10.1002/pd.6056. Epub 2021 Oct 22.
Prenat Diagn. 2022.
PMID: 34643287
Free PMC article.
A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
Corsten-Janssen N, Bouman K, Diphoorn JCD, Scheper AJ, Kinds R, El Mecky J, Breet H, Verheij JBGM, Suijkerbuijk R, Duin LK, Manten GTR, van Langen IM, Sijmons RH, Sikkema-Raddatz B, Westers H, van Diemen CC.
Corsten-Janssen N, et al. Among authors: el mecky j.
Prenat Diagn. 2020 Sep;40(10):1300-1309. doi: 10.1002/pd.5781. Epub 2020 Jul 20.
Prenat Diagn. 2020.
PMID: 32627857
Free PMC article.
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Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists.
El Mecky J, Johansson L, Plantinga M, Fenwick A, Lucassen A, Dijkhuizen T, van der Hout A, Lyle K, van Langen I.
El Mecky J, et al.
BMC Med Genomics. 2019 Nov 29;12(1):170. doi: 10.1186/s12920-019-0612-6.
BMC Med Genomics. 2019.
PMID: 31779608
Free PMC article.
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Support needs of caregivers of patients with amyotrophic lateral sclerosis: A qualitative study.
de Wit J, Schröder CD, El Mecky J, Beelen A, van den Berg LH, Visser-Meily JMA.
de Wit J, et al. Among authors: el mecky j.
Palliat Support Care. 2019 Apr;17(2):195-201. doi: 10.1017/S1478951517001213. Epub 2018 Feb 5.
Palliat Support Care. 2019.
PMID: 29397051
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