Van den Veyver I - Search Results

1

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: van den veyver i. 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.

2

Comparative genomic hybridization and prenatal diagnosis.

Van den Veyver IB, Beaudet AL. Van den Veyver IB, et al. Curr Opin Obstet Gynecol. 2006 Apr;18(2):185-91. doi: 10.1097/01.gco.0000192986.22718.cc. Curr Opin Obstet Gynecol. 2006. PMID: 16601480 Review.

3

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

Sahoo T, Cheung SW, Ward P, Darilek S, Patel A, del Gaudio D, Kang SH, Lalani SR, Li J, McAdoo S, Burke A, Shaw CA, Stankiewicz P, Chinault AC, Van den Veyver IB, Roa BB, Beaudet AL, Eng CM. Sahoo T, et al. Genet Med. 2006 Nov;8(11):719-27. doi: 10.1097/01.gim.0000245576.47154.63. Genet Med. 2006. PMID: 17108764 Free article.

4

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.

Van den Veyver IB, Patel A, Shaw CA, Pursley AN, Kang SH, Simovich MJ, Ward PA, Darilek S, Johnson A, Neill SE, Bi W, White LD, Eng CM, Lupski JR, Cheung SW, Beaudet AL. Van den Veyver IB, et al. Prenat Diagn. 2009 Jan;29(1):29-39. doi: 10.1002/pd.2127. Prenat Diagn. 2009. PMID: 19012303 Free PMC article.

5

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths.

Harris RA, Ferrari F, Ben-Shachar S, Wang X, Saade G, Van Den Veyver I, Facchinetti F, Aagaard-Tillery K. Harris RA, et al. Among authors: van den veyver i. Prenat Diagn. 2011 Oct;31(10):932-44. doi: 10.1002/pd.2817. Epub 2011 Jul 5. Prenat Diagn. 2011. PMID: 21732394 Free PMC article.

6

Copy-number changes in prenatal diagnosis.

Strassberg M, Fruhman G, Van den Veyver IB. Strassberg M, et al. Expert Rev Mol Diagn. 2011 Jul;11(6):579-92. doi: 10.1586/erm.11.43. Expert Rev Mol Diagn. 2011. PMID: 21745012 Review.

7

Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis.

Willis AS, van den Veyver I, Eng CM. Willis AS, et al. Among authors: van den veyver i. Prenat Diagn. 2012 Apr;32(4):315-20. doi: 10.1002/pd.3860. Prenat Diagn. 2012. PMID: 22467161 Review.

8

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

Breman A, Pursley AN, Hixson P, Bi W, Ward P, Bacino CA, Shaw C, Lupski JR, Beaudet A, Patel A, Cheung SW, Van den Veyver I. Breman A, et al. Among authors: van den veyver i. Prenat Diagn. 2012 Apr;32(4):351-61. doi: 10.1002/pd.3861. Prenat Diagn. 2012. PMID: 22467166 Review.

9

Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.

Bi W, Breman A, Shaw CA, Stankiewicz P, Gambin T, Lu X, Cheung SW, Jackson LG, Lupski JR, Van den Veyver IB, Beaudet AL. Bi W, et al. Prenat Diagn. 2012 Jan;32(1):10-20. doi: 10.1002/pd.2855. Prenat Diagn. 2012. PMID: 22470934

10

No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles.

Mahadevan S, Wen S, Balasa A, Fruhman G, Mateus J, Wagner A, Al-Hussaini T, Van den Veyver IB. Mahadevan S, et al. Prenat Diagn. 2013 Dec;33(13):1242-7. doi: 10.1002/pd.4239. Epub 2013 Oct 4. Prenat Diagn. 2013. PMID: 24105752 Free PMC article.

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