Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Daishu Yin"'
Autor:
Lin Chen, Li Wang, Yang Zeng, Daishu Yin, Feng Tang, Dan Xie, Hongmei Zhu, Lingping Li, Jing Wang
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Chimerism results from the fusion of two zygotes in a single embryo, whereas mosaicism results from mitotic errors in a single zygote. True human chimerism is rare, with fewer than 100 cases reported in the literature. Here, we report a case
Externí odkaz:
https://doaj.org/article/817564fb2cb444e984a3c762b635a8e9
Autor:
Lin Chen, Li Wang, Yang Zeng, Daishu Yin, Feng Tang, Dan Xie, Hongmei Zhu, Hongqian Liu, Jing Wang
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Standard noninvasive prenatal screening(NIPS) is an accurate and reliable method to screen for common chromosome aneuploidies, such as trisomy 21, 18 and 13. Extended NIPS has been used in clinic for not only aneuploidies but also
Externí odkaz:
https://doaj.org/article/df38eaeb8c404d14932f6d051ead68ec
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Objective Wolf–Hirschhorn syndrome (WHS) is a congenital malformation syndrome with poor prognosis. It is associated with a heterozygous deletion of chromosome 4p16.3. Adequate knowledge of prenatal phenotypes and proper prenatal counselin
Externí odkaz:
https://doaj.org/article/06d168cd892b4cfba68622144f5b76d6
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-9 (2022)
Abstract Background The broad application of high-resolution chromosome detection technology in prenatal diagnosis has identified copy number loss (CNL) involving autosomal dominant (AD) genes in certain fetuses. Exon sequencing of fetuses exhibiting
Externí odkaz:
https://doaj.org/article/8b1f5899d20841f49e833f5362c5d9d0
Autor:
Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Daishu Yin, Yang Zeng, Feng Tang, Yunyuan Yang, Hongmei Zhu, Xinlian Chen, Qian Zhu, Zhiying Liu, Hongqian Liu
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-7 (2018)
Abstract A prospective analysis investigating the associations between pathogenic copy number variations (pCNVs) and ultrasound soft markers (USMs) in fetuses and evaluating the clinical value of copy number variation sequencing (CNV-seq) in such pre
Externí odkaz:
https://doaj.org/article/c04a9775f08a4724ba2f2486a69aa05e
Autor:
Daishu Yin, Cong Zhou, Yang Zeng, Hongmei Zhu, Li Wang, Jing Wang, Lili Zhang, Feng Tang, Lin Chen, Linping Li
Publikováno v:
J Assist Reprod Genet
PURPOSE: In this study, we evaluated the feasibility of the combining CNV-seq and quantitative fluorescence polymerase chain reaction (QF-PCR) for miscarriage analysis in clinical practice. METHODS: Over a 35-month period, a total of 389 fetal specim
Publikováno v:
Molecular genetics and genomics : MGG. 297(6)
Increased fetal nuchal translucency (NT) is a common ultrasonic manifestation during pregnancy. Many studies have confirmed that NT ≥ 3 mm is a high risk factor for adverse pregnancy outcome. However, when NT is between 2.5 and 2.9 mm, will it incr
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-6 (2020)
Scientific Reports
Scientific Reports
The widespread application of high-resolution chromosome detection technology in clinical practice has identified many variants of unknown significance (VOUS) in prenatal diagnosis. The purpose of this study was to prospectively analyze the chromosom
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Studies on the occurrence of segmental aneuploidoidy in fetuses with isolated echogenic intracardiac focus (EIF) are scarce. The aim of this study was to analyze whether there is an association between abnormal segmental aneuploidies and isolated EIF