Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report

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Veröffentlicht in:Klinická onkologie 2016-01, Vol.29 Suppl 1, p.S89-S92
Hauptverfasser: Puchmajerová, A, Švojgr, K, Novotná, D, Macháčková, E, Sumerauer, D, Smíšek, P, Kodet, R, Kynčl, M, Křepelová, A, etová, L
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container_end_page S92
container_issue
container_start_page S89
container_title Klinická onkologie
container_volume 29 Suppl 1
creator Puchmajerová, A
Švojgr, K
Novotná, D
Macháčková, E
Sumerauer, D
Smíšek, P
Kodet, R
Kynčl, M
Křepelová, A
etová, L
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title Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report
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