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Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.
Preisler B, Pezeshkpoor B, Banchev A, Fischer R, Zieger B, Scholz U, Rühl H, Kemkes-Matthes B, Schmitt U, Redlich A, Unal S, Laws HJ, Olivieri M, Oldenburg J, Pavlova A. Preisler B, et al. Among authors: unal s. J Clin Med. 2021 Jan 18;10(2):347. doi: 10.3390/jcm10020347. J Clin Med. 2021. PMID: 33477601 Free PMC article.
Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations.
Watzka M, Geisen C, Scheer M, Wieland R, Wiegering V, Dörner T, Laws HJ, Gümrük F, Hanalioglu S, Unal S, Albayrak D, Oldenburg J. Watzka M, et al. Among authors: unal s. Thromb Res. 2014 Oct;134(4):856-65. doi: 10.1016/j.thromres.2014.07.004. Epub 2014 Jul 12. Thromb Res. 2014. PMID: 25151188
Fanconi anemia: a single center experience of a large cohort.
Kesici S, Ünal Ş, Kuşkonmaz B, Aytaç S, Çetin M, Gümrük F. Kesici S, et al. Among authors: unal s. Turk J Pediatr. 2019;61(4):477-484. doi: 10.24953/turkjped.2019.04.002. Turk J Pediatr. 2019. PMID: 31990462 Free article.
Kesici S, Unal S, Kuskonmaz B, Aytac S, Cetin M, Gumruk F. Fanconi anemia: a single center experience of a large cohort. ...
Kesici S, Unal S, Kuskonmaz B, Aytac S, Cetin M, Gumruk F. Fanconi anemia: a single center experience of a large …
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.
Tesi B, Lagerstedt-Robinson K, Chiang SC, Ben Bdira E, Abboud M, Belen B, Devecioglu O, Fadoo Z, Yeoh AE, Erichsen HC, Möttönen M, Akar HH, Hästbacka J, Kaya Z, Nunes S, Patiroglu T, Sabel M, Saribeyoglu ET, Tvedt TH, Unal E, Unal S, Unuvar A, Meeths M, Henter JI, Nordenskjöld M, Bryceson YT. Tesi B, et al. Among authors: unal s, unal e. Genome Med. 2015 Dec 18;7:130. doi: 10.1186/s13073-015-0244-1. Genome Med. 2015. PMID: 26684649 Free PMC article.
983 results