Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 12 (of 12 Records) |
Query Trace: Triploidy[original query] |
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Near-triploidy and near-tetraploidy in hematological malignancies and mutation of the p53 gene. Clinical and laboratory haematology 2004 1 26 (1): 25-30. Watanabe A, Inokuchi K, Yamaguchi H, Mizuki T, Tanosaki S, Shimada T, Dan |
Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage. Molecular human reproduction 2013 Aug 19 (8): 539-44. Manokhina I, Hanna C W, Stephenson M D, McFadden D E, Robinson W |
Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception. Genetic testing and molecular biomarkers 2016 May . Zhang HuiMin, Liu WeiQiang, Chen Min, Li ZhiHua, Sun XiaoFang, Wang ChenHo |
[SNP array analysis of three cases with partial 21q trisomy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 12 34 (6): 861-865. Zhou Lili, Chen Chong, Zheng Zhaoke, Wu Hao, Xie Fanni, Lin Xiaoling, Xiang Yanbao, Xu Xueqin, Tang Shaoh |
Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts. Reproductive biomedicine online 2018 1 36 (4): 388-395. Marin Diego, Zimmerman Rebekah, Tao Xin, Zhan Yiping, Scott Richard T, Treff Nathan |
Differentiating diploid and triploid individuals using single nucleotide polymorphisms genotyped by amplicon sequencing. Molecular ecology resources 2019 8 19 (6): 1545-1551. Delomas Thomas |
Single-nucleotide polymorphism microarray detects molar pregnancies in 3% of miscarriages. Fertility and sterility 2019 8 112 (4): 700-706. Maisenbacher Melissa K, Merrion Katrina, Kutteh William |
Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies. Frontiers in genetics 2020 11 571219. Xiang Jingjing, Ding Yang, Song Xiaoyan, Mao Jun, Liu Minjuan, Liu Yinghua, Huang Chao, Zhang Qin, Wang Ti |
Study on the correlation between the ultrasound phenotype and copy number variation of abnormal embryo in spontaneous abortion. The journal of obstetrics and gynaecology research 2021 9 47 (11): 3779-3788. Tan Shuyin, Pan Pingshan, Yang Zuojian, Su Jiasun, Wei Hongw |
Genetic and genomic analysis of acute lymphoblastic leukemia in older adults reveals a distinct profile of abnormalities: analysis of 210 patients from the UKALL14 and UKALL60+ clinical trials. Haematologica 2021 11 107 (9): 2051-2063. Creasey Thomas, Barretta Emilio, Ryan Sarra L, Butler Ellie, Kirkwood Amy A, Leongamornlert Daniel, Papaemmanuil Elli, Patrick Pip, Clifton-Hadley Laura, Patel Bela, Menne Tobias, McMillan Andrew K, Harrison Christine J, Rowntree Clare J, Morley Nick, Marks David I, Fielding Adele K, Moorman Anthony |
Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human. Cytogenetic and genome research 2021 10 161 (8-9): 406-413. He Jian-Chun, Li Shao-Ying, He Wen-Zhi, Xian Jia-Jia, Ma Xiao-Yan, Wang Yan-Chao, Zhang Min-Cong, Ye Guo-Xin, Liang Bo, Xia Qin, Li Qi |
Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism-Based Prenatal Cell-Free DNA Screening. Obstetrics and gynecology 2023 3 . Goldring Georgina, Trotter Cindy, Meltzer Jeffrey T, Souter Vivienne, Pais Lynn, DiNonno Wendy, Xu Wenbo, Weitzel Jeffrey N, Vora Neeta |
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