Langlois S - Search Results

1

Prenatal screening and diagnosis of sex chromosome conditions: The new normal?

Hui L, Langlois S. Hui L, et al. Among authors: langlois s. Prenat Diagn. 2023 Feb;43(2):131-132. doi: 10.1002/pd.6323. Epub 2023 Feb 4. Prenat Diagn. 2023. PMID: 36690923 No abstract available.

2

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.

Kuchinka BD, Barrett IJ, Moya G, Sánchez JM, Langlois S, Yong SL, Kalousek DK, Robinson WP. Kuchinka BD, et al. Among authors: langlois s. Prenat Diagn. 2001 Jan;21(1):36-9. doi: 10.1002/1097-0223(200101)21:1<36::aid-pd979>3.0.co;2-1. Prenat Diagn. 2001. PMID: 11180238

3

Prediction of obstetrical risk using maternal serum markers and clinical risk factors.

Metcalfe A, Langlois S, Macfarlane J, Vallance H, Joseph KS. Metcalfe A, et al. Among authors: langlois s. Prenat Diagn. 2014 Feb;34(2):172-9. doi: 10.1002/pd.4281. Epub 2013 Dec 11. Prenat Diagn. 2014. PMID: 24226970

4

Current controversies in prenatal diagnosis 4: pre-conception expanded carrier screening should replace all current prenatal screening for specific single gene disorders.

Langlois S, Benn P, Wilkins-Haug L. Langlois S, et al. Prenat Diagn. 2015 Jan;35(1):23-8. doi: 10.1002/pd.4532. Prenat Diagn. 2015. PMID: 25395388 No abstract available.

5

Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?

Chitty LS, Friedman JM, Langlois S. Chitty LS, et al. Among authors: langlois s. Prenat Diagn. 2016 Jan;36(1):15-9. doi: 10.1002/pd.4718. Epub 2015 Nov 22. Prenat Diagn. 2016. PMID: 26525746 No abstract available.

6

Current controversies in prenatal diagnosis 2: for those women screened by NIPT using cell free DNA, maternal serum markers are obsolete.

Yaron Y, Hyett J, Langlois S. Yaron Y, et al. Among authors: langlois s. Prenat Diagn. 2016 Dec;36(13):1167-1171. doi: 10.1002/pd.4944. Epub 2016 Nov 15. Prenat Diagn. 2016. PMID: 27747900 No abstract available.

7

Etiologies and outcomes of prenatally diagnosed hyperechogenic kidneys.

Digby EL, Liauw J, Dionne J, Langlois S, Nikkel SM. Digby EL, et al. Among authors: langlois s. Prenat Diagn. 2021 Mar;41(4):465-477. doi: 10.1002/pd.5883. Epub 2021 Jan 3. Prenat Diagn. 2021. PMID: 33337554

8

Current controversies in prenatal diagnosis: Expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered.

Christiaens L, Chitty LS, Langlois S. Christiaens L, et al. Among authors: langlois s. Prenat Diagn. 2021 Sep;41(10):1316-1323. doi: 10.1002/pd.5943. Epub 2021 Jun 15. Prenat Diagn. 2021. PMID: 33829520 Review.

9

Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines.

Cornthwaite M, Turner K, Armstrong L, Boerkoel CF, Chang C, Lehman A, Nikkel SM, Patel MS, Van Allen M, Langlois S. Cornthwaite M, et al. Among authors: langlois s. Prenat Diagn. 2022 Nov;42(12):1514-1524. doi: 10.1002/pd.6232. Epub 2022 Sep 18. Prenat Diagn. 2022. PMID: 36068917

10

Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use.

Vora NL, Langlois S, Chitty LS. Vora NL, et al. Among authors: langlois s. Prenat Diagn. 2024 Apr;44(4):389-397. doi: 10.1002/pd.6469. Epub 2023 Nov 22. Prenat Diagn. 2024. PMID: 37991340 Review.

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