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Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Wapner RJ, Babiarz JE, Levy B, Stosic M, Zimmermann B, Sigurjonsson S, Wayham N, Ryan A, Banjevic M, Lacroute P, Hu J, Hall MP, Demko Z, Siddiqui A, Rabinowitz M, Gross SJ, Hill M, Benn P. Wapner RJ, et al. Among authors: levy b. Am J Obstet Gynecol. 2015 Mar;212(3):332.e1-9. doi: 10.1016/j.ajog.2014.11.041. Epub 2014 Dec 2. Am J Obstet Gynecol. 2015. PMID: 25479548 Free article.
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing.
Vossaert L, Wang Q, Salman R, Zhuo X, Qu C, Henke D, Seubert R, Chow J, U'ren L, Enright B, Stilwell J, Kaldjian E, Yang Y, Shaw C, Levy B, Wapner R, Breman A, Van den Veyver I, Beaudet A. Vossaert L, et al. Among authors: levy b. Prenat Diagn. 2018 Dec;38(13):1069-1078. doi: 10.1002/pd.5377. Epub 2018 Nov 19. Prenat Diagn. 2018. PMID: 30357877 Free PMC article.
Prenatal Diagnosis Using Chromosomal SNP Microarrays.
Ganapathi M, Nahum O, Levy B. Ganapathi M, et al. Among authors: levy b. Methods Mol Biol. 2019;1885:187-205. doi: 10.1007/978-1-4939-8889-1_13. Methods Mol Biol. 2019. PMID: 30506199
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis.
Vossaert L, Wang Q, Salman R, McCombs AK, Patel V, Qu C, Mancini MA, Edwards DP, Malovannaya A, Liu P, Shaw CA, Levy B, Wapner RJ, Bi W, Breman AM, Van den Veyver IB, Beaudet AL. Vossaert L, et al. Among authors: levy b. Am J Hum Genet. 2019 Dec 5;105(6):1262-1273. doi: 10.1016/j.ajhg.2019.11.004. Epub 2019 Nov 27. Am J Hum Genet. 2019. PMID: 31785788 Free PMC article.
2,788 results