Wenzel F - Search Results

1

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

Huang DJ, Nelson MR, Zimmermann B, Dudarewicz L, Wenzel F, Spiegel R, Nagy B, Holzgreve W, Hahn S. Huang DJ, et al. Among authors: wenzel f. Genet Med. 2006 Nov;8(11):728-34. doi: 10.1097/01.gim.0000245573.42908.34. Genet Med. 2006. PMID: 17108765 Free article.

2

Novel real-time quantitative PCR test for trisomy 21.

Zimmermann B, Holzgreve W, Wenzel F, Hahn S. Zimmermann B, et al. Among authors: wenzel f. Clin Chem. 2002 Feb;48(2):362-3. Clin Chem. 2002. PMID: 11805021 No abstract available.

3

Genotyping fetal paternally inherited SNPs by MALDI-TOF MS using cell-free fetal DNA in maternal plasma: influence of size fractionation.

Li Y, Wenzel F, Holzgreve W, Hahn S. Li Y, et al. Among authors: wenzel f. Electrophoresis. 2006 Oct;27(19):3889-96. doi: 10.1002/elps.200600084. Electrophoresis. 2006. PMID: 16972300

4

Detection of SNPs in the plasma of pregnant women and in the urine of kidney transplant recipients by mass spectrometry.

Li Y, Hahn D, Wenzel F, Holzgreve W, Hahn S. Li Y, et al. Among authors: wenzel f. Ann N Y Acad Sci. 2006 Sep;1075:144-7. doi: 10.1196/annals.1368.019. Ann N Y Acad Sci. 2006. PMID: 17108204

5

Cell-free foetal DNA in maternal plasma does not appear to be derived from the rich pool of cell-free foetal DNA in amniotic fluid.

Zhong XY, Holzgreve W, Tercanli S, Wenzel F, Hahn S. Zhong XY, et al. Among authors: wenzel f. Arch Gynecol Obstet. 2006 Jan;273(4):221-6. doi: 10.1007/s00404-005-0068-0. Epub 2005 Sep 28. Arch Gynecol Obstet. 2006. PMID: 16189693

6

Assessing the chromosome copy number in metaphase II oocytes by sequential fluorescence in situ hybridization.

Vollmer M, Wenzel F, DeGeyter C, Zhang H, Holzgreve W, Miny P. Vollmer M, et al. Among authors: wenzel f. J Assist Reprod Genet. 2000 Nov;17(10):596-602. doi: 10.1023/a:1026495527331. J Assist Reprod Genet. 2000. PMID: 11209542 Free PMC article.

7

Mosaic ring chromosome 8: clinical and array-CGH findings in partial trisomy 8.

Filges I, Röthlisberger B, Wenzel F, Heinimann K, Huber AR, Miny P. Filges I, et al. Among authors: wenzel f. Am J Med Genet A. 2008 Nov 1;146A(21):2837-41. doi: 10.1002/ajmg.a.32520. Am J Med Genet A. 2008. PMID: 18924172 No abstract available.

8

Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation family.

Filges I, Röthlisberger B, Noppen C, Boesch N, Wenzel F, Necker J, Binkert F, Huber AR, Heinimann K, Miny P. Filges I, et al. Among authors: wenzel f. Am J Med Genet A. 2009 Feb;149A(2):237-41. doi: 10.1002/ajmg.a.32622. Am J Med Genet A. 2009. PMID: 19161139

9

Fetal polydactyly: a study of 24 cases ascertained by prenatal sonography.

Filges I, Kang A, Hench J, Wenzel F, Bruder E, Miny P, Tercanli S. Filges I, et al. Among authors: wenzel f. J Ultrasound Med. 2011 Jul;30(7):1021-9. doi: 10.7863/jum.2011.30.7.1021. J Ultrasound Med. 2011. PMID: 21705736

10

aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis.

Filges I, Kang A, Klug V, Wenzel F, Heinimann K, Tercanli S, Miny P. Filges I, et al. Among authors: wenzel f. Prenat Diagn. 2011 May;31(5):473-8. doi: 10.1002/pd.2721. Epub 2011 Feb 24. Prenat Diagn. 2011. PMID: 21351283

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