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In-depth characterisation of a cohort of individuals with m..:
Morison, Lottie D
;
Meffert, Elisabeth
;
Stampfer, Miriam
...
Journal of Medical Genetics. 60 (2022) 6 - p. 597-607 , 2022
Link:
https://doi.org/10.1136/jmg-2022-108734
RT Journal T1
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disruptingFOXP2
UL https://suche.suub.uni-bremen.de/peid=cr-10.1136_jmg-2022-108734&Exemplar=1&LAN=DE A1 Morison, Lottie D A1 Meffert, Elisabeth A1 Stampfer, Miriam A1 Steiner-Wilke, Irene A1 Vollmer, Brigitte A1 Schulze, Katrin A1 Briggs, Tracy A1 Braden, Ruth A1 Vogel, Adam A1 Thompson-Lake, Daisy A1 Patel, Chirag A1 Blair, Edward A1 Goel, Himanshu A1 Turner, Samantha A1 Moog, Ute A1 Riess, Angelika A1 Liegeois, Frederique A1 Koolen, David A A1 Amor, David J A1 Kleefstra, Tjitske A1 Fisher, Simon E A1 Zweier, Christiane A1 Morgan, Angela T PB BMJ YR 2022 SN 0022-2593 SN 1468-6244 JF Journal of Medical Genetics VO 60 IS 6 SP 597 OP 607 LK http://dx.doi.org/https://doi.org/10.1136/jmg-2022-108734 DO https://doi.org/10.1136/jmg-2022-108734 SF ELIB - SuUB Bremen
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