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Dive into the research topics of 'Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation'. Together they form a unique fingerprint.- Sort by
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Paweł Stankiewicz, Alma Kuechler, C. Daniel Eller, Trilochan Sahoo, Christiane Baldermann, Ulla Lieser, Martin Hesse, Christiane Gläser, Monika Hagemann, Svetlana A. Yatsenko, Thomas Liehr, Bernhard Horsthemke, Uwe Claussen, York Marahrens, James R. Lupski, Ingo Hansmann
Research output: Contribution to journal › Article › peer-review