Vestergaard EM - Search Results

1

Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings.

Vestergaard EM, Christensen R, Petersen OB, Vogel I. Vestergaard EM, et al. Acta Obstet Gynecol Scand. 2013 Jul;92(7):762-8. doi: 10.1111/aogs.12146. Epub 2013 May 9. Acta Obstet Gynecol Scand. 2013. PMID: 23590624 Free article.

2

Diagnostic performance of quantitative fluorescence PCR analysis in high-risk pregnancies after combined first-trimester screening.

Lildballe DL, Vogel I, Petersen OB, Vestergaard EM. Lildballe DL, et al. Among authors: vestergaard em. Dan Med J. 2014 Nov;61(11):A4964. Dan Med J. 2014. PMID: 25370964 Free article.

3

Chromosomal microarray in fetuses with increased nuchal translucency.

Lund IC, Christensen R, Petersen OB, Vogel I, Vestergaard EM. Lund IC, et al. Among authors: vestergaard em. Ultrasound Obstet Gynecol. 2015 Jan;45(1):95-100. doi: 10.1002/uog.14726. Ultrasound Obstet Gynecol. 2015. PMID: 25393210 Free article.

4

Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray.

Lund IC, Vestergaard EM, Christensen R, Uldbjerg N, Becher N. Lund IC, et al. Among authors: vestergaard em. Eur J Med Genet. 2016 Jan;59(1):48-51. doi: 10.1016/j.ejmg.2015.12.001. Epub 2015 Dec 9. Eur J Med Genet. 2016. PMID: 26679067

5

17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature.

Rasmussen M, Vestergaard EM, Graakjaer J, Petkov Y, Bache I, Fagerberg C, Kibaek M, Svaneby D, Petersen OB, Brasch-Andersen C, Sunde L. Rasmussen M, et al. Among authors: vestergaard em. Am J Med Genet A. 2016 Nov;170(11):2934-2942. doi: 10.1002/ajmg.a.37848. Epub 2016 Jul 13. Am J Med Genet A. 2016. PMID: 27409573 Review.

6

Non-invasive prenatal testing offered as part of a combined first-trimester screening program identifies tetrasomy 18p in a high-risk pregnancy.

Lildballe DL, Vogel I, Lund IC, Stornes I, Jørgensen MW, Vestergaard EM. Lildballe DL, et al. Among authors: vestergaard em. Prenat Diagn. 2016 Dec;36(12):1112-1114. doi: 10.1002/pd.4943. Epub 2016 Nov 10. Prenat Diagn. 2016. PMID: 27743407 No abstract available.

7

First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray.

Støve HK, Becher N, Gjørup V, Ramsing M, Vogel I, Vestergaard EM. Støve HK, et al. Among authors: vestergaard em. Clin Case Rep. 2017 Mar 17;5(5):608-612. doi: 10.1002/ccr3.902. eCollection 2017 May. Clin Case Rep. 2017. PMID: 28469860 Free PMC article.

8

Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population-based combined first-trimester screening program.

Vogel I, Petersen OB, Christensen R, Hyett J, Lou S, Vestergaard EM. Vogel I, et al. Among authors: vestergaard em. Ultrasound Obstet Gynecol. 2018 Apr;51(4):480-486. doi: 10.1002/uog.17548. Epub 2018 Mar 4. Ultrasound Obstet Gynecol. 2018. PMID: 28608362 Free article.

9

On the road to replacing invasive testing with cell-based NIPT: Five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement, or mosaicism.

Vestergaard EM, Singh R, Schelde P, Hatt L, Ravn K, Christensen R, Lildballe DL, Petersen OB, Uldbjerg N, Vogel I. Vestergaard EM, et al. Prenat Diagn. 2017 Nov;37(11):1120-1124. doi: 10.1002/pd.5150. Epub 2017 Oct 10. Prenat Diagn. 2017. PMID: 28881392

10

Case of successful IVF treatment of an oligospermic male with 46,XX/46,XY chimerism.

Laursen RJ, Alsbjerg B, Vogel I, Gravholt CH, Elbaek H, Lildballe DL, Humaidan P, Vestergaard EM. Laursen RJ, et al. Among authors: vestergaard em. J Assist Reprod Genet. 2018 Jul;35(7):1325-1328. doi: 10.1007/s10815-018-1194-5. Epub 2018 Apr 30. J Assist Reprod Genet. 2018. PMID: 29713857 Free PMC article.

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