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1 Ergebnisse
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Xq22 deletions and correlation with distinct neurological d..:
Hijazi, Hadia
;
Coelho, Fernanda S.
;
Gonzaga‐Jauregui, Claudia
...
Human Mutation. 41 (2019) 1 - p. 150-168 , 2019
Link:
https://doi.org/10.1002/humu.23902
RT Journal T1
Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_humu.23902&Exemplar=1&LAN=DE A1 Hijazi, Hadia A1 Coelho, Fernanda S. A1 Gonzaga‐Jauregui, Claudia A1 Bernardini, Laura A1 Mar, Soe S. A1 Manning, Melanie A. A1 Hanson‐Kahn, Andrea A1 Naidu, SakkuBai A1 Srivastava, Siddharth A1 Lee, Jennifer A. A1 Jones, Julie R. A1 Friez, Michael J. A1 Alberico, Thomas A1 Torres, Barbara A1 Fang, Ping A1 Cheung, Sau Wai A1 Song, Xiaofei A1 Davis‐Williams, Angelique A1 Jornlin, Carly A1 Wight, Patricia A. A1 Patyal, Pankaj A1 Taube, Jennifer A1 Poretti, Andrea A1 Inoue, Ken A1 Zhang, Feng A1 Pehlivan, Davut A1 Carvalho, Claudia M. B. A1 Hobson, Grace M. A1 Lupski, James R. PB Hindawi Limited YR 2019 SN 1059-7794 SN 1098-1004 JF Human Mutation VO 41 IS 1 SP 150 OP 168 LK http://dx.doi.org/https://doi.org/10.1002/humu.23902 DO https://doi.org/10.1002/humu.23902 SF ELIB - SuUB Bremen
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