Results 101 to 110 of about 7,985 (170)

Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family. [PDF]

Mol Cytogenet, 2022
Zhang Y, Chen J, Feng Z, Li W.
europepmc   +1 more source

Mosaic distal 10q deletion or 46,XY,del(10) (q26.13)/46,XY at amniocentesis and cordocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome

Objective: We present mosaic distal 10q deletion at prenatal diagnosis in a pregnancy associated with a favorable fetal outcome. Case report: A 40-year-old, gravida 2, para 0, woman underwent amniocentesis at 16 weeks of gestation because of advanced ...
Fang-Tzu Wu, Wayseen Wang, Yen-Ting Pan, Chien-Ling Chiu, Chih-Ping Chen, Peih-Shan Wu, Wen-Lin Chen, Liang-Kai Wang, Chen-Chi Lee   +8 more
core   +1 more source

Prenatal diagnosis and follow-up of a child with mosaic tetrasomy 9p without obvious abnormal clinical manifestations. [PDF]

Mol Cytogenet
Zhang L, Qian F, Chen W, Fan J, Zeng Y, Luo T, Che M, Yu B, Zhang T.   +8 more
europepmc   +1 more source

Chromosomal structural abnormalities and tissue-specific mosaicism: insights into false-negative noninvasive prenatal testing. [PDF]

Front Genet
Huang N, Xu Y, Ding S, Pan L, Zhou P, Zou Y, Feng C, Huang S, Liu Y, Yang B, Yuan H.   +10 more
europepmc   +1 more source

A fetus with paternal uniparental isodisomy of chromosome 3: genetic analysis and prenatal diagnosis following a positive NIPS with IUGR. [PDF]

Mol Cytogenet
Zhang F, Ma S, Wang Y, Men S, Zhang R, Yin T.   +5 more
europepmc   +1 more source

Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype. [PDF]

Mol Cytogenet, 2022
Song J, Jiang W, Zhang C, Wang B.
europepmc   +1 more source

Low-level mosaic trisomy 6 at amniocentesis can be a culture artefact and associated with a favorable outcome and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes

Taiwanese Journal of Obstetrics and Gynecology, 2023
openaire   +3 more sources

Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review. [PDF]

Medicine (Baltimore), 2023
Lv X, Yang X, Li L, Yue F, Zhang H, Wang R.   +5 more
europepmc   +1 more source

Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 5p13.3p13.2 microduplication in a Chinese family. [PDF]

Mol Cytogenet
Wang W, Zhan L, Xu L, Leng P.
europepmc   +1 more source

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome

, 2018
[[abstract]]Objective We present prenatal diagnosis of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome. Case Report A 40-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced ...
陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Pan, Chen-Wen;Wang, Wayseen
core