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1 Ergebnisse
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Rare coding variants as risk modifiers of the 22q11.2 delet..:
Lin, Jhih-Rong
;
Zhao, Yingjie
;
Jabalameli, M. Reza
...
Molecular Psychiatry. 28 (2023) 5 - p. 2071-2080 , 2023
Link:
https://doi.org/10.1038/s41380-023-02009-y
RT Journal T1
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41380-023-02009-y&Exemplar=1&LAN=DE A1 Lin, Jhih-Rong A1 Zhao, Yingjie A1 Jabalameli, M. Reza A1 Nguyen, Nha A1 Mitra, Joydeep A1 Swillen, Ann A1 Vorstman, Jacob A. S. A1 Chow, Eva W. C. A1 van den Bree, Marianne A1 Emanuel, Beverly S. A1 Vermeesch, Joris R. A1 Owen, Michael J. A1 Williams, Nigel M. A1 Bassett, Anne S. A1 McDonald-McGinn, Donna M. A1 Gur, Raquel E. A1 Bearden, Carrie E. A1 Morrow, Bernice E. A1 Lachman, Herbert M. A1 Zhang, Zhengdong D. A1 International 22q11.DS Brain and Behavior Consortium PB Springer Science and Business Media LLC YR 2023 SN 1359-4184 SN 1476-5578 JF Molecular Psychiatry VO 28 IS 5 SP 2071 OP 2080 LK http://dx.doi.org/https://doi.org/10.1038/s41380-023-02009-y DO https://doi.org/10.1038/s41380-023-02009-y SF ELIB - SuUB Bremen
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