Kang A - Search Results

1

Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries.

Meier N, Bruder E, Lapaire O, Hoesli I, Kang A, Hench J, Hoeller S, De Geyter J, Miny P, Heinimann K, Chaoui R, Tercanli S, Filges I. Meier N, et al. Among authors: kang a. Eur J Hum Genet. 2019 May;27(5):730-737. doi: 10.1038/s41431-018-0324-y. Epub 2019 Jan 24. Eur J Hum Genet. 2019. PMID: 30679815 Free PMC article.

2

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: kang a. J Ultrasound Med. 2011 Jul;30(7):1021-9. doi: 10.7863/jum.2011.30.7.1021. J Ultrasound Med. 2011. PMID: 21705736

3

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: kang a. Prenat Diagn. 2011 May;31(5):473-8. doi: 10.1002/pd.2721. Epub 2011 Feb 24. Prenat Diagn. 2011. PMID: 21351283

4

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies.

Filges I, Kang A, Klug V, Wenzel F, Heinimann K, Tercanli S, Miny P. Filges I, et al. Among authors: kang a. Mol Cytogenet. 2012 Sep 17;5(1):38. doi: 10.1186/1755-8166-5-38. Mol Cytogenet. 2012. PMID: 22979998 Free PMC article.

5

Is a routine ultrasound in the third trimester justified? Additional fetal anomalies diagnosed after two previous unremarkable ultrasound examinations.

Manegold G, Tercanli S, Struben H, Huang D, Kang A. Manegold G, et al. Among authors: kang a. Ultraschall Med. 2011 Aug;32(4):381-6. doi: 10.1055/s-0029-1245799. Epub 2011 Feb 3. Ultraschall Med. 2011. PMID: 21294069

6

[Prenatal diagnosis of diastematomyelia and tethered cord - a case report and review of the literature].

Struben H, Visca E, Holzgreve W, Kang A, Hetzel P, Schneider J, Tercanli S. Struben H, et al. Among authors: kang a. Ultraschall Med. 2008 Feb;29(1):72-6. doi: 10.1055/s-2007-963208. Epub 2007 Oct 10. Ultraschall Med. 2008. PMID: 17926255 German.

7

Prenatal diagnosis of a case of ectrodactyly in 2D and 3D ultrasound.

Kang A, Visca E, Bruder E, Holzgreve W, Struben H, Tercanli S. Kang A, et al. Ultraschall Med. 2009 Apr;30(2):121-3. doi: 10.1055/s-0029-1220169. Epub 2009 Apr 17. Ultraschall Med. 2009. PMID: 19421951 English, German. No abstract available.

8

Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms.

Li Y, Zimmermann B, Rusterholz C, Kang A, Holzgreve W, Hahn S. Li Y, et al. Among authors: kang a. Clin Chem. 2004 Jun;50(6):1002-11. doi: 10.1373/clinchem.2003.029835. Epub 2004 Apr 8. Clin Chem. 2004. PMID: 15073090

9

Both maternal and fetal cell-free DNA in plasma fluctuate.

Hahn S, Zhong XY, Bürk MR, Troeger C, Kang A, Holzgreve W. Hahn S, et al. Among authors: kang a. Ann N Y Acad Sci. 2001 Sep;945:141-4. doi: 10.1111/j.1749-6632.2001.tb03875.x. Ann N Y Acad Sci. 2001. PMID: 11708468 Review.

10

Inability to detect cell free fetal DNA in the urine of normal pregnant women nor in those affected by preeclampsia associated HELLP syndrome.

Li Y, Zhong XY, Kang A, Troeger C, Holzgreve W, Hahn S. Li Y, et al. Among authors: kang a. J Soc Gynecol Investig. 2003 Dec;10(8):503-8. doi: 10.1016/s1071-5576(03)00155-2. J Soc Gynecol Investig. 2003. PMID: 14662164

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