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Muramatsu, Hideki; Okuno, Yusuke; Yoshida, Kenichi; Shiraishi, Yuichi; Doisaki, Sayoko; Narita, Atsushi; Sakaguchi, Hirotoshi; Kawashima, Nozomu; Wang, Xinan; Xu, Yinyan; Chiba, Kenichi; Tanaka, Hiroko; Hama, Asahito; Sanada, Masashi; Takahashi, Yoshiyuki; Kanno, Hitoshi; Yamaguchi, Hiroki; Ohga, Shouichi; Manabe, Atsushi; Harigae, Hideo; Kunishima, Shinji; Ishii, Eiichi; Kobayashi, Masao; Koike, Kenichi; Watanabe, Kenichiro; Ito, Etsuro; Takata, Minoru; Yabe, Miharu; Ogawa, Seishi; Miyano, Satoru; Kojima, Seiji
Genetics in medicine, 07/2017, Letnik: 19, Številka: 7Journal Article
Precise genetic diagnosis of inherited bone marrow failure syndromes (IBMFS), a heterogeneous group of genetic disorders, is challenging but essential for precise clinical decision making. We analyzed 121 IBMFS patients using a targeted sequencing covering 184 associated genes and 250 IBMFS patients using whole-exome sequencing (WES). We achieved successful genetic diagnoses for 53 of 121 patients (44%) using targeted sequencing and for 68 of 250 patients (27%) using WES. In the majority of cases (targeted sequencing: 45/53, 85%; WES: 63/68, 93%), the detected variants were concordant with, and therefore supported, the clinical diagnoses. However, in the remaining 13 cases (8 patients by target sequencing and 5 patients by WES), the clinical diagnoses were incompatible with the detected variants. Our approach utilizing targeted sequencing and WES achieved satisfactory diagnostic rates and supported the efficacy of massive parallel sequencing as a diagnostic tool for IBMFS.Genet Med advance online publication 19 January 2017.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Vir: Osebne bibliografije
in: SICRIS
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