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1070 related items for PubMed ID: 26384064
21. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism. Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W. Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380 [Abstract] [Full Text] [Related]
24. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus. Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Chen LF, Wang W. Taiwan J Obstet Gynecol; 2021 May; 60(3):534-539. PubMed ID: 33966743 [Abstract] [Full Text] [Related]
25. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes. Chen CP, Lo LM, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Chen LF, Chen YY, Wang W. Taiwan J Obstet Gynecol; 2021 Mar; 60(2):331-334. PubMed ID: 33678337 [Abstract] [Full Text] [Related]
28. Low-level mosaic trisomy 21 at amniocentesis 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. Chen CP, Wu FT, Pan YT, Wu PS, Pan CW, Wang W. Taiwan J Obstet Gynecol; 2023 Nov; 62(6):910-914. PubMed ID: 38008514 [Abstract] [Full Text] [Related]
29. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy. Chen CP, Chern SR, Wang LK, Wu PS, Wu FT, Chen YY, Town DD, Pan CW, Wang W. Taiwan J Obstet Gynecol; 2020 Nov; 59(6):938-940. PubMed ID: 33218416 [Abstract] [Full Text] [Related]
30. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome. Chen CP, Lin SY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. Taiwan J Obstet Gynecol; 2020 Mar; 59(2):301-305. PubMed ID: 32127154 [Abstract] [Full Text] [Related]
31. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16. Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W. Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616 [Abstract] [Full Text] [Related]
32. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis. Chen CP, Chang SD, Su YN, Chen M, Chern SR, Su JW, Chen YT, Chen WL, Pan CW, Lee MS, Wang W. Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926 [Abstract] [Full Text] [Related]
35. Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome. Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Chen YY, Wang W. Taiwan J Obstet Gynecol; 2022 Jan; 61(1):141-145. PubMed ID: 35181026 [Abstract] [Full Text] [Related]
36. Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterine growth restriction, intrauterine fetal death, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line. Chen CP, Wu FT, Chen YY, Pan YT, Wu PS, Lee MS, Pan CW, Wang W. Taiwan J Obstet Gynecol; 2023 Jul; 62(4):597-601. PubMed ID: 37407203 [Abstract] [Full Text] [Related]
38. Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome. Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. Taiwan J Obstet Gynecol; 2017 Dec; 56(6):840-842. PubMed ID: 29241931 [Abstract] [Full Text] [Related]
39. Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome. Chen CP, Wu FT, Pan YT, Wu PS, Chen WL, Lee CC, Wang W. Taiwan J Obstet Gynecol; 2023 Nov; 62(6):891-895. PubMed ID: 38008510 [Abstract] [Full Text] [Related]
40. Prenatal diagnosis of mosaicism for double trisomies of trisomy 11 and trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Wang W. Taiwan J Obstet Gynecol; 2020 May; 59(3):443-445. PubMed ID: 32416896 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]