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Ehret JK, Engels H, Cremer K, et al. Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. Mol Cytogenet. 2015;8:72doi: 10.1186/s13039-015-0178-8.
Ehret, J. K., Engels, H., Cremer, K., Becker, J., Zimmermann, J. P., Wohlleber, E., Grasshoff, U., Rossier, E., Bonin, M., Mangold, E., Bevot, A., Schön, S., Heilmann-Heimbach, S., Dennert, N., Mathieu-Dramard, M., Lacaze, E., Plessis, G., de Broca, A., Jedraszak, G., Röthlisberger, B., Miny, P., Filges, I., Dufke, A., Andrieux, J., Lee, J. A., & Zink, A. M. (2015). Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. Molecular cytogenetics, 872. https://doi.org/10.1186/s13039-015-0178-8
Ehret, Julia K, et al. "Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?." Molecular cytogenetics vol. 8 (2015): 72. doi: https://doi.org/10.1186/s13039-015-0178-8
Ehret JK, Engels H, Cremer K, Becker J, Zimmermann JP, Wohlleber E, Grasshoff U, Rossier E, Bonin M, Mangold E, Bevot A, Schön S, Heilmann-Heimbach S, Dennert N, Mathieu-Dramard M, Lacaze E, Plessis G, de Broca A, Jedraszak G, Röthlisberger B, Miny P, Filges I, Dufke A, Andrieux J, Lee JA, Zink AM. Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. Mol Cytogenet. 2015 Sep 29;8:72. doi: 10.1186/s13039-015-0178-8. eCollection 2015. PMID: 26421060; PMCID: PMC4587785.
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