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1دورية أكاديمية
المؤلفون: Ping Wei, Weizhe Shi, Tianying Nong, Caixia Xian, Xia Li, Zhaohui Li, Xin Li, Jianping Wu, Liyuan Shang, Fulong Xu, Yibo Xu, Hongwen Xu, Mingwei Zhu
المصدر: Genes and Diseases, Vol 11, Iss 3, Pp 101006- (2024)
مصطلحات موضوعية: Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S2352304223002635Test; https://doaj.org/toc/2352-3042Test
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2دورية أكاديمية
المؤلفون: Yue Li, Tianying Nong, Yiqiang Li, Xia Li, Zhaohui Li, Hui Lv, Hongwen Xu, Jingchun Li, Mingwei Zhu
المصدر: Molecular Genetics & Genomic Medicine, Vol 10, Iss 12, Pp n/a-n/a (2022)
مصطلحات موضوعية: distal arthrogryposis, TNNI2, variant, whole‐exome sequencing, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2324-9269Test
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3دورية أكاديمية
المؤلفون: Caixia Xian, Mingwei Zhu, Tianying Nong, Yiqiang Li, Xingmei Xie, Xia Li, Jiangui Li, Jingchun Li, Jianping Wu, Weizhe Shi, Ping Wei, Hongwen Xu, Ya-ping Tang
المصدر: Genetics and Molecular Biology, Vol 44, Iss 2 (2021)
مصطلحات موضوعية: Osteochondroma, hereditary, EXT1, EXT2, heparan sulfate, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.scielo.br/pdf/gmb/v44n2/1415-4757-GMB-44-2-e20200334.pdfTest; http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000300112&tlng=enTest; https://doaj.org/toc/1678-4685Test
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المؤلفون: Caixia Xian, HongWen Xu, Mingwei Zhu, Weizhe Shi, YiQiang Li, Xingmei Xie, Jiangui Li, Xia Li, Jianping Wu, Ya-Ping Tang, Ping Wei, JingChun Li, Tianying Nong
المصدر: Genetics and Molecular Biology
Genetics and Molecular Biology v.44 n.2 2021
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 44, Iss 2 (2021)
Genetics and Molecular Biology, Volume: 44, Issue: 2, Article number: e20200334, Published: 21 MAY 2021مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Osteochondroma, Hereditary multiple exostoses, QH426-470, Biology, 01 natural sciences, Frameshift mutation, 03 medical and health sciences, chemistry.chemical_compound, Exon, Skeletal disorder, Genetics, medicine, Molecular Biology, Exome sequencing, Splice site mutation, EXT2, Heparan sulfate, EXT1, medicine.disease, Stop codon, 030104 developmental biology, chemistry, Human and Medical Genetics, heparan sulfate, hereditary, 010606 plant biology & botany
وصف الملف: text/html
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97ef73660860e9d61548e9cce8634a7Test
https://pubmed.ncbi.nlm.nih.gov/34042151Test