Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yunrong Qin"'
Autor:
Yinghong Lu, Na Zuo, Minxia Ning, Yuling Xie, Weiwu Liu, Sisi Ning, Yi Liang, Xiao Chen, Yuping Zhang, Jun Feng, Yunrong Qin
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Increased sequencing depth can improve the detection rate of noninvasive prenatal testing (NIPT) for chromosome aneuploidies and copy number variations (CNVs). However, due to the technical limitations of NIPT, false-positives and false-nega
Externí odkaz:
https://doaj.org/article/8cf401322b4646f0b571cbbb841bde9b
Autor:
Yinghong Lu, Yi Liang, Sisi Ning, Guosheng Deng, Yuling Xie, Jujie Song, Na Zuo, Chunfeng Feng, Yunrong Qin
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-8 (2020)
Abstract Background Small supernumerary marker chromosomes (sSMCs), are additional abnormal chromosomes, which can’t be detected accurately by banding cytogenetic analysis. Abnormal phenotypes were observed in about 30% of SMC carriers. Duplication
Externí odkaz:
https://doaj.org/article/07f0eaddf03445cdabf39bc6c03bc878
Autor:
Sisi Ning, Yudi Luo, Yi Liang, Yuling Xie, Yinghong Lu, Binrong Meng, Jinjie Pan, Ruofan Xu, Yinyin Liu, Yunrong Qin
Publikováno v:
Clinica Chimica Acta. 535:7-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e68c8053868f0b3089d77874b1311f46
https://doi.org/10.1016/j.cca.2022.07.020
https://doi.org/10.1016/j.cca.2022.07.020
Autor:
Sisi Ning, Yunrong Qin, Yunning Liang, Yi Liang, Yuling Xie, Yinghong Lu, Guanghong Wei, Ruofan Xu, Yinyin Liu, Jihui Li
Publikováno v:
Gene. 875:147505
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acf281a022a22c20c6da699de89a0a8e
https://doi.org/10.1016/j.gene.2023.147505
https://doi.org/10.1016/j.gene.2023.147505
Autor:
Yuling Xie, Yinghong Lu, Chunfeng Feng, Jujie Song, Guosheng Deng, Yi Liang, Yunrong Qin, Sisi Ning, Na Zuo
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-8 (2020)
Molecular Cytogenetics
Molecular Cytogenetics
Background Small supernumerary marker chromosomes (sSMCs), are additional abnormal chromosomes, which can’t be detected accurately by banding cytogenetic analysis. Abnormal phenotypes were observed in about 30% of SMC carriers. Duplication of chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0966ac823ee33cc29372a8e9513834d5
http://link.springer.com/article/10.1186/s13039-020-00489-z
http://link.springer.com/article/10.1186/s13039-020-00489-z
Autor:
Sisi, Ning, Yudi, Luo, Yi, Liang, Yuling, Xie, Yinghong, Lu, Binrong, Meng, Jinjie, Pan, Ruofan, Xu, Yinyin, Liu, Yunrong, Qin
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 535
Thalassemia is one of the most common hemoglobinopathies. Thalassemia is mainly caused by the loss and/or deficiency of one or more globin chains in hemoglobin. The copy number variant (CNV) of α-globin gene is one of the important factors affecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb7a7721bc7feaa38a6e36c8f6e5427d
https://pubmed.ncbi.nlm.nih.gov/35944700
https://pubmed.ncbi.nlm.nih.gov/35944700