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Items: 1 to 20 of 171

1.

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. doi: 10.1016/j.gene.2013.07.048. Epub 2013 Aug 7. Review.

PMID:
23933412
2.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.

Chen CP, Ko TM, Chen YY, Su JW, Wang W.

Gene. 2013 Sep 15;527(1):384-8. doi: 10.1016/j.gene.2013.05.061. Epub 2013 Jun 6.

PMID:
23747353
3.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.

Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W.

Taiwan J Obstet Gynecol. 2012 Sep;51(3):411-7. doi: 10.1016/j.tjog.2012.07.017.

5.

Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.

Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W.

Gene. 2013 Oct 15;529(1):163-8. doi: 10.1016/j.gene.2013.07.050. Epub 2013 Aug 8.

PMID:
23933417
6.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.

Chen CP, Chen M, Su YN, Tsai FJ, Chern SR, Wu PC, Chen WL, Chen LF, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2011 Jun;50(2):188-95. doi: 10.1016/j.tjog.2011.04.002.

7.

Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.

Chen CP, Chiang S, Wang KL, Cho FN, Chen M, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2016 Jun;55(3):419-22. doi: 10.1016/j.tjog.2016.05.002.

8.

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.

Prenat Diagn. 2006 Oct;26(10):898-902.

PMID:
16915592
9.

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. doi: 10.1016/j.gene.2013.09.025. Epub 2013 Sep 18. Review.

PMID:
24055486
10.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.

Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2016 Dec;55(6):852-855. doi: 10.1016/j.tjog.2016.08.002.

11.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.

Chen CP, Chen M, Ko TM, Ma GC, Tsai FJ, Tsai MS, Wu PC, Lee CC, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2010 Dec;49(4):500-5. doi: 10.1016/S1028-4559(10)60104-0.

12.

Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.

Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2013 Mar;52(1):97-105. doi: 10.1016/j.tjog.2013.01.012. Review.

13.

Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.

Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2016 Oct;55(5):728-732. doi: 10.1016/j.tjog.2016.06.017.

14.

Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W.

Taiwan J Obstet Gynecol. 2011 Mar;50(1):67-73. doi: 10.1016/j.tjog.2011.01.038.

15.

Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.

Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM.

Cytogenet Genome Res. 2009;125(2):109-14. doi: 10.1159/000227834. Epub 2009 Aug 31.

PMID:
19729913
16.

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. doi: 10.1016/j.tjog.2013.06.004.

17.

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;51(2):245-52. doi: 10.1016/j.tjog.2012.04.015.

18.

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.

Chen CP, Chern SR, Chen YN, Wu PS, Yang CW, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2015 Aug;54(4):426-31. doi: 10.1016/j.tjog.2015.06.002. Review.

19.

Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.

Chen CP, Su JW, Chern SR, Kuo YL, Wu PS, Lee MS, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2015 Feb;54(1):58-61. doi: 10.1016/j.tjog.2014.12.002.

20.

Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.

Chen CP, Lin CC, Li YC, Chern SR, Lee CC, Chen WL, Lee MS, Wang W, Tzen CY.

Prenat Diagn. 2004 Oct;24(10):767-73. Review.

PMID:
15503270

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