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1 Ergebnisse
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Identification of novel rare copy number variants associate..:
He, Guo‐Wei
;
Maslen, Cheryl L.
;
Chen, Huan‐Xin
...
Clinical Genetics. 102 (2022) 5 - p. 391-403 , 2022
Link:
https://doi.org/10.1111/cge.14201
RT Journal T1
Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14201&Exemplar=1&LAN=DE A1 He, Guo‐Wei A1 Maslen, Cheryl L. A1 Chen, Huan‐Xin A1 Hou, Hai‐Tao A1 Bai, Xiao‐Yan A1 Wang, Xiu‐Li A1 Liu, Xiao‐Cheng A1 Lu, Wan‐Li A1 Chen, Xin‐Xin A1 Chen, Wei‐Dan A1 Xing, Quan‐Sheng A1 Wu, Qin A1 Wang, Jun A1 Yang, Qin PB Wiley YR 2022 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 102 IS 5 SP 391 OP 403 LK http://dx.doi.org/https://doi.org/10.1111/cge.14201 DO https://doi.org/10.1111/cge.14201 SF ELIB - SuUB Bremen
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