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Journal Abstract Search

247 related items for PubMed ID: 32039782

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  • 3. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
    Chen CP, Liou JD, Seow KM, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
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  • 4. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP, Wang YL, Chern SR, Liu YP, Peng CR, Kuo YL, Wu PS, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
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  • 6. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
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  • 10. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
    Chen CP, Chang SY, Wang LK, Chang TY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Town DD, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):730-733. PubMed ID: 30342661
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  • 11. Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Chuang TY, Wang W.
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):869-871. PubMed ID: 31759545
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  • 12. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
    Chen CP, Liou JD, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):146-149. PubMed ID: 35181027
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  • 13. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Wang W.
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):165-168. PubMed ID: 33494995
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  • 15. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication.
    Chen CP, Huang JP, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):140-145. PubMed ID: 32039783
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  • 17. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
    Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):692-697. PubMed ID: 31542095
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  • 19. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
    Chen CP, Chang SY, Lin CJ, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):734-738. PubMed ID: 30342662
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