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Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome
- Nishimura, A (author)
- Hirabayashi, S (author)
- Hasegawa, D (author)
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- Yoshida, K (author)
- Shiraishi, Y (author)
- Ashiarai, M (author)
- Hosoya, Y (author)
- Fujiwara, T (author)
- Harigae, H (author)
- Miyano, S (author)
- Ogawa, S (author)
- Manabe, A (author)
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- 2020-11-16
- 2021
- English.
- In: Pediatric blood & cancer. - : Wiley. - 1545-5017 .- 1545-5009. ; 68:2, s. e28799-
- Journal article (peer-reviewed)
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- Nishimura, A
- Hirabayashi, S
- Hasegawa, D
- Yoshida, K
- Shiraishi, Y
- Ashiarai, M
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- Hosoya, Y
- Fujiwara, T
- Harigae, H
- Miyano, S
- Ogawa, S
- Manabe, A
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- Karolinska Institutet
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