Stumm M - Search Results

1

Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe.

Stumm M, Entezami M, Haug K, Blank C, Wüstemann M, Schulze B, Raabe-Meyer G, Hempel M, Schelling M, Ostermayer E, Langer-Freitag S, Burkhardt T, Zimmermann R, Schleicher T, Weil B, Schöck U, Smerdka P, Grömminger S, Kumar Y, Hofmann W. Stumm M, et al. Prenat Diagn. 2014 Feb;34(2):185-91. doi: 10.1002/pd.4278. Epub 2013 Dec 12. Prenat Diagn. 2014. PMID: 24222400

2

Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms.

Stumm M, Entezami M, Trunk N, Beck M, Löcherbach J, Wegner RD, Hagen A, Becker R, Hofmann W. Stumm M, et al. Prenat Diagn. 2012 Jun;32(6):569-77. doi: 10.1002/pd.3862. Epub 2012 May 9. Prenat Diagn. 2012. PMID: 22573401

3

The influence of low molecular weight heparin medication on plasma DNA in pregnant women.

Grömminger S, Erkan S, Schöck U, Stangier K, Bonnet J, Schloo R, Schubert A, Prott EC, Knoll U, Stumm M, von Kalle C, Hofmann W. Grömminger S, et al. Among authors: stumm m. Prenat Diagn. 2015 Nov;35(11):1155-7. doi: 10.1002/pd.4668. Epub 2015 Sep 4. Prenat Diagn. 2015. PMID: 26248743 No abstract available.

4

Non-invasive prenatal diagnosis using massively parallel sequencing - first experience in Germany.

Wegner RD, Stumm M, Hofmann W. Wegner RD, et al. Among authors: stumm m. Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I14. doi: 10.1186/1755-8166-7-S1-I14. eCollection 2014. Mol Cytogenet. 2014. PMID: 24955117 Free PMC article. No abstract available.

5

[Prenatal diagnostics: current medical aspects].

Stumm M, Entezami M. Stumm M, et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013 Dec;56(12):1662-9. doi: 10.1007/s00103-013-1854-7. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013. PMID: 24337128 Review. German.

6

Fetal 46,XX/69,XXY mixoploidy: origin and confirmation by analysis of fetal urine cells.

Wegner RD, Kistner G, Becker R, Stumm M, Knoll U, Entezami M, Trimborn M. Wegner RD, et al. Among authors: stumm m. Prenat Diagn. 2009 Mar;29(3):287-9. doi: 10.1002/pd.2213. Prenat Diagn. 2009. PMID: 19194868 No abstract available.

7

Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins.

Grömminger S, Yagmur E, Erkan S, Nagy S, Schöck U, Bonnet J, Smerdka P, Ehrich M, Wegner RD, Hofmann W, Stumm M. Grömminger S, et al. Among authors: stumm m. J Clin Med. 2014 Jun 25;3(3):679-92. doi: 10.3390/jcm3030679. J Clin Med. 2014. PMID: 26237471 Free PMC article.

8

Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis.

Stumm M, Klopocki E, Gasiorek-Wiens A, Knoll U, Wirjadi D, Sarioglu N, Wegner RD, Tönnies H. Stumm M, et al. Prenat Diagn. 2007 May;27(5):475-8. doi: 10.1002/pd.1703. Prenat Diagn. 2007. PMID: 17330228 Review.

9

The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age.

Hagen A, Entezami M, Gasiorek-Wiens A, Albig M, Becker R, Knoll U, Stumm M, Wegner RD. Hagen A, et al. Among authors: stumm m. Ultraschall Med. 2011 Jun;32(3):302-6. doi: 10.1055/s-0029-1245560. Epub 2010 Oct 22. Ultraschall Med. 2011. PMID: 20972947

10

Suspicious Prenasal Skin Thickness-to-Nasal Bone Length Ratio: Prevalence and Correlation with Other Markers in Second and Third Trimester Fetuses with Down Syndrome.

Hagen A, Albig M, Keller T, Stumm M, Entezami M. Hagen A, et al. Among authors: stumm m. Ultraschall Med. 2015 Oct;36(5):501-6. doi: 10.1055/s-0034-1399285. Epub 2015 Jun 19. Ultraschall Med. 2015. PMID: 26091004

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