Resultados de procura - Marie Trková

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  1. 1
    BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations

    BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations por Anindita Basak, Miroslava Hančárová, Jacob C. Ulirsch, Tuğçe B. Balcı, Marie Trková, Michal Pelisek, Markéta Vlčková, Kateřina Mužíková, Jaroslav Čermák, Jan Trka, David A. Dyment, Stuart H. Orkin, Mark J. Daly, Zdeněk Sedláček, Vijay G. Sankaran

    Publicado 2015
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  2. 2
    Monitoring of childhood ALL using BCR-ABL1 genomic breakpoints identifies a subgroup with CML-like biology

    Monitoring of childhood ALL using BCR-ABL1 genomic breakpoints identifies a subgroup with CML-like biology por Lenka Hovorková, Markéta Žaliová, Nicola C. Venn, Kirsten Bleckmann, Marie Trková, Eliška Potůčková, Martina Vášková, Jana Linhartová, Kateřina Machová Poláková, Eva Froňková, Walter Muskovic, Jodie E. Giles, Peter J. Shaw, Gunnar Cario, Rosemary Sutton, Jan Starý, Jan Trka, Jan Zuna

    Publicado 2017
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  3. 3
    Axenfeld-Rieger syndrome: more than meets the eye

    Axenfeld-Rieger syndrome: more than meets the eye por Linda M. Reis, Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Ľubica Ďuďáková, Samuel Thompson, Lia Zitano, Guillermo Lay‐Son, R. Brian Lowry, Jennifer D. Black, Joseph Lee, Ann Shue, Radka Kremlíková Pourová, Manuela Vaněčková, Pavlína Skalická, Jana Jedličková, Marie Trková, Bradley A. Williams, Gabriele Richard, Kristine Bachman, Andrea Seeley, Deborah M. Costakos, Thomas Gläser, Alex V. Levin, Petra Lišková, Jeffrey C. Murray, Elena V. Semina

    Publicado 2022
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