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Comment
. 2019 Oct;39(11):1039-1040.
doi: 10.1002/pd.5522. Epub 2019 Sep 10.

Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?

Karin Diderich  1 , Marieke Joosten  1 , Lutgarde Govaerts  1 , Diane Van Opstal  1 , Attie Go  2 , Maarten Knapen  2 , Robert-Jan Galjaard  1 , Lies Hoefsloot  1 , Malgorzata Srebniak  1
Affiliations
Comment

Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?

Karin Diderich et al. Prenat Diagn. 2019 Oct.
No abstract available

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Comment on

  • Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.

References

    1. Lord J, McMullan DJ, Eberhardt RY, et al. G. Prenatal Assessment of and C. Exomes. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study. Lancet. 2019;393(10173):747‐757. - PMC - PubMed
    1. Petrovski S, Aggarwal V, Giordano JL, et al. Whole‐exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study. Lancet. 2019;393(10173):758‐767. - PubMed
    1. D. International Society for Prenatal, M. Society for, M. Fetal and F. Perinatal Quality . Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome‐wide sequencing for fetal diagnosis. Prenat Diagn. 2018;38(1):6‐9. - PubMed