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per Sampath Kumar, Abhishek, Seah, Michelle K.Y., Ling, Ka Yi, Wang, Yaju, Tan, Joel H.L., Nitsch, Sandra, Lim, Shu Ly, Lorthongpanich, Chanchao, Wollmann, Heike, Low, Diana H.P., Guccione, Ernesto, Messerschmidt, Daniel M.
Publicat a Genes Dev (2017)
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PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly
per Mzoughi, Slim, Di Tullio, Federico, Low, Diana H. P., Motofeanu, Corina-Mihaela, Ong, Sheena L. M., Wollmann, Heike, Wun, Cheng Mun, Kruszka, Paul, Muenke, Maximilian, Hildebrandt, Friedhelm, Dunn, N. Ray, Messerschmidt, Daniel M., Guccione, Ernesto
Publicat a Sci Adv (2020)
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per Seah, Michelle K. Y., Wang, Yaju, Goy, Pierre-Alexis, Loh, Hui Mun, Peh, Wen Jun, Low, Diana H. P., Han, Brenda Y., Wong, Esther, Leong, Ei Leen, Wolf, Gernot, Mzoughi, Slim, Wollmann, Heike, Macfarlan, Todd S., Guccione, Ernesto, Messerschmidt, Daniel M.
Publicat a Development (2019)
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per Dewaele, Michael, Tabaglio, Tommaso, Willekens, Karen, Bezzi, Marco, Teo, Shun Xie, Low, Diana H.P., Koh, Cheryl M., Rambow, Florian, Fiers, Mark, Rogiers, Aljosja, Radaelli, Enrico, Al-Haddawi, Muthafar, Tan, Soo Yong, Hermans, Els, Amant, Frederic, Yan, Hualong, Lakshmanan, Manikandan, Koumar, Ratnacaram Chandrahas, Lim, Soon Thye, Derheimer, Frederick A., Campbell, Robert M., Bonday, Zahid, Tergaonkar, Vinay, Shackleton, Mark, Blattner, Christine, Marine, Jean-Christophe, Guccione, Ernesto
Publicat a J Clin Invest (2015)
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