The 22q11.2 deletion syndrome: Cancer predisposition, platelet abnormalities and cytopenias
Lambert, Michele P., Arulselvan, Abinaya, Schott, Amanda, Markham, Stephen J., Crowley, Terrance B., Zackai, Elaine H., McDonald‐McGinn, Donna M.
Published in American journal of medical genetics. Part A (01.10.2018)
Published in American journal of medical genetics. Part A (01.10.2018)
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Integrated molecular and clinical analysis of low-grade gliomas in children with neurofibromatosis type 1 (NF1)
Fisher, Michael J., Jones, David T. W., Li, Yimei, Guo, Xiaofan, Sonawane, Poonam S., Waanders, Angela J., Phillips, Joanna J., Weiss, William A., Resnick, Adam C., Gosline, Sara, Banerjee, Jineta, Guinney, Justin, Gnekow, Astrid, Kandels, Daniela, Foreman, Nicholas K., Korshunov, Andrey, Ryzhova, Marina, Massimi, Luca, Gururangan, Sri, Kieran, Mark W., Wang, Zhihong, Fouladi, Maryam, Sato, Mariko, Øra, Ingrid, Holm, Stefan, Markham, Stephen J., Beck, Pengbo, Jäger, Natalie, Wittmann, Andrea, Sommerkamp, Alexander C., Sahm, Felix, Pfister, Stefan M., Gutmann, David H.
Published in Acta neuropathologica (01.04.2021)
Published in Acta neuropathologica (01.04.2021)
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Detecting 22q11.2 Deletion Syndrome Using Flow Cytometry
Markham, Stephen J, Bevilaqua, Lisa, Zarrin, Haley, McDonald-McGinn, Donna, Zackai, Elaine, Lambert, Michele P
Published in Blood (06.12.2014)
Published in Blood (06.12.2014)
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