Skip to main content
Haematologica logoLink to Haematologica
. 2020 Apr;105(4):1166–1167. doi: 10.3324/haematol.2019.245720

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

Minako Mori 1,2, Asuka Hira 1, Kenichi Yoshida 3, Hideki Muramatsu 4, Yusuke Okuno 4, Yuichi Shiraishi 5, Michiko Anmae 6, Jun Yasuda 7, Shu Tadaka 7, Kengo Kinoshita 7,8,9, Tomoo Osumi 10, Yasushi Noguchi 11, Souichi Adachi 12, Ryoji Kobayashi 13, Hiroshi Kawabata 14, Kohsuke Imai 15, Tomohiro Morio 16, Kazuo Tamura 6, Akifumi Takaori-Kondo 2, Masayuki Yamamoto 7,17, Satoru Miyano 5, Seiji Kojima 4, Etsuro Ito 18, Seishi Ogawa 3,19, Keitaro Matsuo 20, Hiromasa Yabe 21, Miharu Yabe 21, Minoru Takata 1
PMCID: PMC7109714  PMID: 32238468

An incorrected version of table 2 appared On October 2019 Issue, page 1967. The corrected version of table 2 is published on the next page.

Table 2.

Clinical phenotype of 10 Japanese Fanconi anemia patients with VACTERL-H association.

graphic file with name 1051166.tab2.jpg


Articles from Haematologica are provided here courtesy of Ferrata Storti Foundation

RESOURCES