Similar articles for PMID: 23933412

Year	Number of Results
1966	1
1993	2
1995	2
1996	2
1997	1
1998	2
1999	3
2000	1
2001	2
2002	1
2003	7
2004	4
2005	5
2006	10
2007	9
2008	3
2009	6
2010	14
2011	17
2012	13
2013	32
2014	17
2015	15
2016	10
2017	13
2018	10
2019	11
2020	11
2021	7
2022	9
2023	1
2024	0

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. Chen CP, et al. Gene. 2013 Oct 15;529(1):169-75. doi: 10.1016/j.gene.2013.07.048. Epub 2013 Aug 7. Gene. 2013. PMID: 23933412 Review.

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. Chen CP, et al. Gene. 2013 Sep 15;527(1):384-8. doi: 10.1016/j.gene.2013.05.061. Epub 2013 Jun 6. Gene. 2013. PMID: 23747353

3

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2016 Dec;55(6):852-855. doi: 10.1016/j.tjog.2016.08.002. Taiwan J Obstet Gynecol. 2016. PMID: 28040132 Free article.

4

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2012 Sep;51(3):411-7. doi: 10.1016/j.tjog.2012.07.017. Taiwan J Obstet Gynecol. 2012. PMID: 23040927 Free article.

5

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2012 Sep;51(3):405-10. doi: 10.1016/j.tjog.2012.07.016. Taiwan J Obstet Gynecol. 2012. PMID: 23040926 Free article.

6

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. Chen CP, et al. Gene. 2013 Oct 15;529(1):163-8. doi: 10.1016/j.gene.2013.07.050. Epub 2013 Aug 8. Gene. 2013. PMID: 23933417

7

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.

Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chang SP, Yang CW, Pan CW, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2017 Aug;56(4):527-533. doi: 10.1016/j.tjog.2017.06.002. Taiwan J Obstet Gynecol. 2017. PMID: 28805612 Free article.

8

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2011 Jun;50(2):188-95. doi: 10.1016/j.tjog.2011.04.002. Taiwan J Obstet Gynecol. 2011. PMID: 21791306 Free article.

9

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2016 Jun;55(3):419-22. doi: 10.1016/j.tjog.2016.05.002. Taiwan J Obstet Gynecol. 2016. PMID: 27343327 Free article.

10

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. Lin CC, et al. Prenat Diagn. 2006 Oct;26(10):898-902. doi: 10.1002/pd.1520. Prenat Diagn. 2006. PMID: 16915592

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