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Journal Abstract Search
299 related items for PubMed ID: 24055486
1. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W. Gene; 2013 Dec 10; 532(1):80-6. PubMed ID: 24055486 [Abstract] [Full Text] [Related]
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 10; 59(5):758-762. PubMed ID: 32917332 [Abstract] [Full Text] [Related]
4. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review. Chen CP, Chen M, Su YN, Huang JP, Chern SR, Wu PS, Su JW, Chang SP, Chen YT, Lee CC, Chen LF, Pan CW, Wang W. Gene; 2013 Oct 15; 529(1):169-75. PubMed ID: 23933412 [Abstract] [Full Text] [Related]
5. Increased first-trimester nuchal translucency associated with a dicentric chromosome and 9q34.3 microdeletion syndrome. Huang LY, Yang Y, He P, Li DZ. J Obstet Gynaecol; 2017 Apr 15; 37(3):327-329. PubMed ID: 27966372 [Abstract] [Full Text] [Related]
8. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry. Chen CP, Su YN, Lin SP, Chern SR, Su JW, Chen YT, Lee MS, Wang W. Taiwan J Obstet Gynecol; 2013 Mar 15; 52(1):120-4. PubMed ID: 23548232 [Abstract] [Full Text] [Related]
9. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result. Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. Taiwan J Obstet Gynecol; 2021 Jul 15; 60(4):775-777. PubMed ID: 34247824 [Abstract] [Full Text] [Related]
10. 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 15; 52(3):395-400. PubMed ID: 24075380 [Abstract] [Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry. Chen CP, Hwang KS, Su HY, Lin SP, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Wang W. Taiwan J Obstet Gynecol; 2013 Mar 15; 52(1):125-8. PubMed ID: 23548233 [Abstract] [Full Text] [Related]
14. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Chen CP, Chen M, Su YN, Huang JP, Ma GC, Chang SP, Chern SR, Chen YT, Su JW, Lee CC, Town DD, Wang W. Taiwan J Obstet Gynecol; 2012 Jun 15; 51(2):245-52. PubMed ID: 22795102 [Abstract] [Full Text] [Related]
15. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect. Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Chen YT, Su JW, Wang W. Gene; 2013 Dec 01; 531(2):496-501. PubMed ID: 24036431 [Abstract] [Full Text] [Related]
16. A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus. Sismani C, Donoghue J, Alexandrou A, Karkaletsi M, Christopoulou S, Konstantinidou AE, Livanos P, Patsalis PC, Velissariou V. Gene; 2013 Nov 01; 530(1):138-42. PubMed ID: 23973723 [Abstract] [Full Text] [Related]
17. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion. Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Lee MS, Yang CW, Wang W. Taiwan J Obstet Gynecol; 2016 Oct 01; 55(5):705-711. PubMed ID: 27751420 [Abstract] [Full Text] [Related]