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1 Ergebnisse
1
Whole exome sequencing identified a homozygous novel varian..:
Zhang, Rui
;
Chen, Shaoyun
;
Han, Peng
...
Journal of Cellular and Molecular Medicine. 24 (2019) 2 - p. 1906-1916 , 2019
Link:
https://doi.org/10.1111/jcmm.14887
RT Journal T1 <Title>Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_jcmm.14887&Exemplar=1&LAN=DE A1 Zhang, Rui A1 Chen, Shaoyun A1 Han, Peng A1 Chen, Fangfang A1 Kuang, Shan A1 Meng, Zhuo A1 Liu, Junnian A1 Sun, Ruliang A1 Wang, Zhiwei A1 He, Xiaohong A1 Li, Yong A1 Guan, Yuanning A1 Yue, Zhengfang A1 Li, Chen A1 Kumar Dey, Subrata A1 Zhu, Yuanfang A1 Banerjee, Santasree PB Wiley YR 2019 SN 1582-1838 SN 1582-4934 JF Journal of Cellular and Molecular Medicine VO 24 IS 2 SP 1906 OP 1916 LK http://dx.doi.org/https://doi.org/10.1111/jcmm.14887 DO https://doi.org/10.1111/jcmm.14887 SF ELIB - SuUB Bremen
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