Sarioglu N - Search Results

1

Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13.

Trimborn M, Wegner RD, Tönnies H, Sarioglu N, Albig M, Neitzel H. Trimborn M, et al. Among authors: sarioglu n. Prenat Diagn. 2006 Mar;26(3):273-6. doi: 10.1002/pd.1396. Prenat Diagn. 2006. PMID: 16506262

2

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. Among authors: sarioglu n. Prenat Diagn. 2007 May;27(5):475-8. doi: 10.1002/pd.1703. Prenat Diagn. 2007. PMID: 17330228 Review.

3

First-trimester prenatal diagnosis of Okihiro syndrome.

Becker R, Horn D, Knoll U, Stumm M, Wegner RD, Peters H, Sarioglu N. Becker R, et al. Among authors: sarioglu n. Fetal Diagn Ther. 2010;27(4):222-6. doi: 10.1159/000287252. Epub 2010 Feb 17. Fetal Diagn Ther. 2010. PMID: 20160433

4

Epignathus: always a simple teratoma? Report of an exceptional case with two additional fetiforme bodies.

Sarioglu N, Wegner RD, Gasiorek-Wiens A, Entezami M, Schmock J, Hagen A, Becker R. Sarioglu N, et al. Ultrasound Obstet Gynecol. 2003 Apr;21(4):397-403. doi: 10.1002/uog.92. Ultrasound Obstet Gynecol. 2003. PMID: 12704752 Free article.

5

[Massive placental hemorrhage in partial molar pregnancy due to hypotriploidy (68,XX)--prenatal diagnosis and clinical course].

Henrich W, Schmider A, Sarioglu N, Neitzel H. Henrich W, et al. Among authors: sarioglu n. Z Geburtshilfe Neonatol. 2001 May-Jun;205(3):114-6. doi: 10.1055/s-2001-15769. Z Geburtshilfe Neonatol. 2001. PMID: 11474990 German.

6

Early diagnosis of conjoined twins by real-time three-dimensional ultrasound--case report and review of the literature.

Schmid O, Hagen A, Sarioglu N, Hopp H, Entezami M, Albig M, Becker R. Schmid O, et al. Among authors: sarioglu n. Ultraschall Med. 2006 Aug;27(4):384-8. doi: 10.1055/s-2005-858357. Epub 2006 Apr 13. Ultraschall Med. 2006. PMID: 16612786 Review.

7

Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4.

Neitzel H, Varon R, Chughtai S, Dartsch J, Dutrannoy-Tönsing V, Nürnberg P, Nürnberg G, Schweiger M, Digweed M, Hildebrand G, Hackmann K, Holtgrewe M, Sarioglu N, Schulze B, Horn D, Sperling K. Neitzel H, et al. Among authors: sarioglu n. Hum Genet. 2022 Nov;141(11):1785-1794. doi: 10.1007/s00439-022-02461-w. Epub 2022 May 10. Hum Genet. 2022. PMID: 35536377 Free PMC article.

8

Prenatal diagnosis of a nasal cyst in association with deletion 22q11 syndrome: a report of two cases.

Karl K, Creton F, Thiel G, Sarioglu N, Heling KS, Chaoui R. Karl K, et al. Among authors: sarioglu n. Prenat Diagn. 2011 Oct;31(10):999-1001. doi: 10.1002/pd.2812. Epub 2011 Jun 28. Prenat Diagn. 2011. PMID: 21710588 No abstract available.

9

Mirror syndrome: a systematic review of fetal associated conditions, maternal presentation and perinatal outcome.

Braun T, Brauer M, Fuchs I, Czernik C, Dudenhausen JW, Henrich W, Sarioglu N. Braun T, et al. Among authors: sarioglu n. Fetal Diagn Ther. 2010;27(4):191-203. doi: 10.1159/000305096. Epub 2010 Mar 27. Fetal Diagn Ther. 2010. PMID: 20357423 Review.

10

Novel Insights in Fetal Cardiomyopathy due to in utero Herpes Simplex Virus Infection.

Pahlitzsch TMJ, Helbig ET, Sarioglu N, Hinkson L, von Weizsäcker K, Henrich W. Pahlitzsch TMJ, et al. Among authors: sarioglu n. Fetal Diagn Ther. 2017;42(3):236-239. doi: 10.1159/000475814. Epub 2017 May 16. Fetal Diagn Ther. 2017. PMID: 28505611

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