Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency von Riedhammer, Korbinian M, Burgemeister, Anna L, Cantagrel, Vincent, Amiel, Jeanne, Siquier-Pernet, Karine, Boddaert, Nathalie, Hertecant, Jozef, Kannouche, Patricia L, Pouvelle, Caroline, Htun, Stephanie, Slavotinek, Anne M, Beetz, Christian, Diego-Alvarez, Dan, Kampe, Kapil, Fleischer, Nicole, Awamleh, Zain, Weksberg, Rosanna, Kopajtich, Robert, Meitinger, Thomas, Suleiman, Jehan, El-Hattab, Ayman W

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Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demean... von Suleiman, Jehan, Riedhammer, Korbinian M., Jicinsky, Timothy, Mundt, Melinda, Werner, Laurie, Gusic, Mirjana, Burgemeister, Anna L., Alsaif, Hessa S., Abdulrahim, Maha, Moghrabi, Nabil N, Nicolas‐Jilwan, Manal, AlSayed, Moeenaldeen, Bi, Weimin, Sampath, Srirangan, Alkuraya, Fowzan S., El‐Hattab, Ayman W.

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Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum von Burgemeister, Anna L., Daumiller, Eva, du Bois, Gabriele, Graul-Neumann, Luitgard M., Köhler, Birgit, Knecht, Susanne, Burgemeister, Stefan, Gronwald, Sarah, Maurer, Martin H., Zirn, Birgit

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Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency von Riedhammer, Korbinian M, Burgemeister, Anna L, Amiel, Jeanne, Cantagrel, Vincent, Siquier-Pernet, Karine, Boddaert, Nathalie, Hertecant, Jozef, Kannouche, Patricia L, Pouvelle, Caroline, Htun, Stephanie, Slavotinek, Anne M, Diego-Alvarez, Dan, Beetz, Christian, Kampe, Kapil, Fleischer, Nicole, Awamleh, Zain, Weksberg, Rosanna, Meitinger, Thomas, Kopajtich, Robert, Suleiman, Jehan, El-Hattab, Ayman W

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