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100 | 1 | _ | |0 P:(DE-82)748672 |a Kirschner, Martin |b 0 |u rwth |
245 | _ | _ | |a Novel homozygous nonsense mutation in the P5′N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling |h online |
260 | _ | _ | |a Chichester |b Wiley |c 2022 |
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700 | 1 | _ | |0 P:(DE-82)IDM06178 |a Koschmieder, Steffen |b 2 |u rwth |
700 | 1 | _ | |a Manco, Licinio |b 3 |
700 | 1 | _ | |a Bento, Celeste |b 4 |
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700 | 1 | _ | |0 P:(DE-82)021451 |a Jost, Edgar |b 7 |u rwth |
700 | 1 | _ | |0 P:(DE-82)IDM06025 |a Brümmendorf, Tim Henrik |b 8 |u rwth |
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773 | _ | _ | |0 PERI:(DE-600)2740234-4 |a 10.1002/ccr3.5501 |n 3 |p e05501 |t Clinical Case Reports |v 10 |x 2050-0904 |
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