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Dual independent genetic etiologies in a lethal complex malformation phenotype.
Filges I, Genewein A, Weber P, Meier S, Deigendesch N, Bruder E, Prüfer F, Tercanli S. Filges I, et al. Among authors: tercanli s. Ultraschall Med. 2020 Apr;41(2):112-114. doi: 10.1055/a-1104-3625. Epub 2020 Apr 7. Ultraschall Med. 2020. PMID: 32259861 English. No abstract available.
An Appeal for Ultrasound and Current Guidelines.
Tercanli S, Filges I. Tercanli S, et al. Ultraschall Med. 2015 Oct;36(5):424-6. doi: 10.1055/s-0035-1553777. Epub 2015 Oct 15. Ultraschall Med. 2015. PMID: 26468769 No abstract available.
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: tercanli s. 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.
How genomics is changing the practice of prenatal testing.
Filges I, Miny P, Holzgreve W, Tercanli S. Filges I, et al. Among authors: tercanli s. J Perinat Med. 2021 Jul 1;49(8):1003-1010. doi: 10.1515/jpm-2021-0220. Print 2021 Oct 26. J Perinat Med. 2021. PMID: 34214293 Free article.
113 results