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Variants in PHF8 cause a spectrum of X-linked neurodevelopm..:
Sobering, Andrew K.
;
Bryant, Laura M.
;
Li, Dong
...
Human Genetics and Genomics Advances. 3 (2022) 3 - p. 100102 , 2022
Link:
https://doi.org/10.1016/j.xhgg.2022.100102
RT Journal T1
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.xhgg.2022.100102&Exemplar=1&LAN=DE A1 Sobering, Andrew K. A1 Bryant, Laura M. A1 Li, Dong A1 McGaughran, Julie A1 Maystadt, Isabelle A1 Moortgat, Stephanie A1 Graham Jr., John M. A1 van Haeringen, Arie A1 Ruivenkamp, Claudia A1 Cuperus, Roos A1 Vogt, Julie A1 Morton, Jenny A1 Brasch-Andersen, Charlotte A1 Steenhof, Maria A1 Hansen, Lars Kjærsgaard A1 Adler, Élodie A1 Lyonnet, Stanislas A1 Pingault, Veronique A1 Sandrine, Marlin A1 Ziegler, Alban A1 Donald, Tyhiesia A1 Nelson, Beverly A1 Holt, Brandon A1 Petryna, Oleksandra A1 Firth, Helen A1 McWalter, Kirsty A1 Zyskind, Jacob A1 Telegrafi, Aida A1 Juusola, Jane A1 Person, Richard PB Elsevier BV YR 2022 SN 2666-2477 JF Human Genetics and Genomics Advances VO 3 IS 3 SP 100102 LK http://dx.doi.org/https://doi.org/10.1016/j.xhgg.2022.100102 DO https://doi.org/10.1016/j.xhgg.2022.100102 SF ELIB - SuUB Bremen
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