Prenatal diagnosis and genetic analysis of small supernumerary marker chromosomes in the eastern chinese han population: A retrospective study of 36 cases-Reference-Cited by-同舟云学术

Prenatal diagnosis and genetic analysis of small supernumerary marker chromosomes in the eastern chinese han population: A retrospective study of 36 cases

Published:2024-07-19 Issue:3 Volume:32 Page:
ISSN:1573-6849
Container-title:Chromosome Research
language:en
Short-container-title:Chromosome Res

Author:

Jiang Xiali,Liang Bin,Chen Bilian,Wu Xiaoqing,Wang Yan,Lin Na,Huang Hailong,Xu Liangpu

Funder

Joints Funds for the Innovation of Science and Technology, Fujian Province

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10577-024-09754-y.pdf

Reference29 articles.

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2. Chen CP, Lin CJ, Chen SW, Wu FT, Chern SR, Wu PS, Chen YY, Chen WL, Wang W (2020) Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia. Taiwan J Obstet Gynecol 59:941–944. https://doi.org/10.1016/j.tjog.2020.09.024

3. D’Ambrosio F, Chan JT, Aslam H, Aguirre Castaneda R, De Simone L, Shad Z (2019) Turner syndrome due to Xp22.33 deletion with preserved gonadal function: case report. Oxf Med Case Reports omz028:5. https://doi.org/10.1093/omcr/omz028

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5. Gohring I, Blumlein HM, Hoyer J, Ekici AB, Trautmann U, Rauch A (2008) 6.7 Mb interstitial duplication in chromosome band 11q24.2q25 associated with infertility, minor dysmorphic features and normal psychomotor development. Eur J Med Genet 51:666–671. https://doi.org/10.1016/j.ejmg.2008.07.009