Central venous catheter placement at the time of extracorporeal membrane oxygenation decannulation: is it safe? von Rauth, Thomas P, Scott, B. Paul, Thomason, Cynthia K, Bartilson, Randall E, Hann, Tracy M, Pietsch, John B

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Smoothened Mutation Confers Resistance to a Hedgehog Pathway Inhibitor in Medulloblastoma von Yauch, Robert L., Dijkgraaf, Gerrit J. P., Alicke, Bruno, Januario, Thomas, Ahn, Christina P., Holcomb, Thomas, Pujara, Kanan, Stinson, Jeremy, Callahan, Christopher A., Tang, Tracy, Bazan, J. Fernando, Kan, Zhengyan, Seshagiri, Somasekar, Hann, Christine L., Gould, Stephen E., Low, Jennifer A., Rudin, Charles M., de Sauvage, Frederic J.

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Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia von Rohanizadegan, Mersedeh, Tracy, Sarah, Galarreta, Carolina I., Poorvu, Tabitha, Buchmiller, Terry L., Bird, Lynne M., Estroff, Judy A., Tan, Wen‐Hann

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N., Clark, Karl J., Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B., Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E., Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H., Klee, Eric W., Engleman, Kendra, Safina, Nicole P., Slaugh, Rachel, Bryant, Emily M., Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N., Schaefer, G. Bradley, Towner, Shelley, Brilstra, Eva H., Koeleman, Bobby P. C.

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N, Clark, Karl J, Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B, Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E, Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H, Klee, Eric W, Engleman, Kendra, Safina, Nicole P, Slaugh, Rachel, Bryant, Emily M, Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N, Schaefer, G Bradley, Towner, Shelley, Brilstra, Eva H, Koeleman, Bobby P C

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Prospective gene expression analysis accurately subtypes acute leukaemia in children and establishes a commonality between hyperdiploidy and t(12;21) in acute lymphoblastic leukaem... von Delft, Frederik W., Bellotti, Tony, Luo, Zhiyuan, Jones, Louise K., Patel, Naina, Yiannikouris, Olga, Hill, Alex S., Hubank, Mike, Kempski, Helena, Fletcher, Danielle, Chaplin, Tracy, Foot, Nicola, Young, Bryan D., Hann, Ian M., Gammerman, Alex, Saha, Vaskar

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N, Clark, Karl J, Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B, Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E, Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H, Klee, Eric W, Engleman, Kendra, Safina, Nicole P, Slaugh, Rachel, Bryant, Emily M, Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N, Schaefer, G. Bradley, Towner, Shelley, Brilstra, Eva H, Koeleman, Bobby P. C

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