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1 Ergebnisse
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De Novo ZMYND8 variants result in an autosomal dominant neu..:
Dias, Kerith-Raie
;
Carlston, Colleen M
;
Blok, Laura E
...
NHMRC APP1117394. , 2022
Link:
https://doi.org/10.1016/j.gim.2022.06.001
RT Journal T1
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
UL https://suche.suub.uni-bremen.de/peid=base-ftunivwestsyd:oai:researchdirect.westernsydney.edu.au:uws_69527&Exemplar=1&LAN=DE A1 Dias, Kerith-Raie A1 Carlston, Colleen M A1 Blok, Laura E A1 De Hayr, Lachlan A1 Nawaz, Urwah A1 Evans, Carey-Anne A1 Bayrak-Toydemir, Pinar A1 Htun, Stephanie A1 Zhu, Ying A1 Ma, Alan A1 Lynch, Sally A A1 Moorwood, Catherine A1 Stals, Karen A1 Ellard, Sian A1 Bainbridge, Matthew N A1 Friedman, Jennifer A1 Pappas, John G A1 Rabin, Rachel A1 Nowak, Catherine B A1 Douglas, Jessica A1 Wilson, Theodore E A1 Guillen Sacoto, Maria J A1 Mullegama, Sureni V A1 Palculict, Timothy B A1 Kirk, Edwin P A1 Pinner, Jason A1 Edwards, Matthew (R16367) A1 Montanari, Francesca A1 Graziano, Claudio A1 Pippucci, Tommaso A1 Dingmann, Bri A1 Glass, Ian A1 Mefford, Heather C A1 Shimoji, Takeyoshi A1 Suzuki, Toshimitsu A1 Yamakawa, Kazuhiro A1 Streff, Haley A1 Schaaf, Christian P A1 Slavotinek, Anne M A1 Voineagu, Irina A1 Carey, John C A1 Buckley, Michael F A1 Schenck, Annette A1 Harvey, Robert J A1 Roscioli, Tony PB U.S., Elsevier YR 2022 K1 320213 - Medical genetics (excl. cancer genetics) K1 200101 - Diagnosis of human diseases and conditions JF NHMRC APP1117394 LK http://dx.doi.org/https://doi.org/10.1016/j.gim.2022.06.001 DO https://doi.org/10.1016/j.gim.2022.06.001 SF ELIB - SuUB Bremen
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