Chen YJ - Search Results

1

Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.

Chen CP, Lin SP, Chern SR, Chen YJ, Tsai FJ, Wu PC, Wang W. Chen CP, et al. Among authors: chen yj. Eur J Med Genet. 2010 Jul-Aug;53(4):217-20. doi: 10.1016/j.ejmg.2010.03.006. Epub 2010 Mar 24. Eur J Med Genet. 2010. PMID: 20346423

2

Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chen CP, Kuo YT, Lin SP, Su YN, Chen YJ, Hsueh RY, Lin YH, Wu PC, Lee CC, Chen YT, Wang W. Chen CP, et al. Among authors: chen yj, chen yt. Taiwan J Obstet Gynecol. 2010 Sep;49(3):327-32. doi: 10.1016/S1028-4559(10)60069-1. Taiwan J Obstet Gynecol. 2010. PMID: 21056319 Free article.

3

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.

Chen CP, Lin SP, Lin CC, Chen YJ, Chern SR, Li YC, Hsieh LJ, Lee CC, Pan CW, Wang W. Chen CP, et al. Among authors: chen yj. Am J Med Genet A. 2006 Jul 15;140(14):1594-600. doi: 10.1002/ajmg.a.31329. Am J Med Genet A. 2006. PMID: 16770806 Review.

4

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.

Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W. Chen CP, et al. Among authors: chen yj, chen m. Prenat Diagn. 2006 Aug;26(8):725-9. doi: 10.1002/pd.1496. Prenat Diagn. 2006. PMID: 16927391

5

Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.

Chen CP, Wang TH, Chen YJ, Chang TY, Liu YP, Tzen CY, Chern SR, Wang W. Chen CP, et al. Among authors: chen yj. Prenat Diagn. 2007 Oct;27(10):967-9. doi: 10.1002/pd.1797. Prenat Diagn. 2007. PMID: 17602449 No abstract available.

6

Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis.

Sung PL, Cheng EE, Chen YJ, Chern SR, Shih CY, Chang CM, Wang PH, Yen MS, Huang CY, Chen CP. Sung PL, et al. Among authors: chen yj, chen cp. Taiwan J Obstet Gynecol. 2013 Dec;52(4):602-6. doi: 10.1016/j.tjog.2013.10.030. Taiwan J Obstet Gynecol. 2013. PMID: 24411055 Free article. No abstract available.

7

Functional independence of Taiwanese patients with mucopolysaccharidoses.

Lee CL, Lin HY, Chuang CK, Chiu HC, Tu RY, Huang YH, Hwu WL, Tsai FJ, Chiu PC, Niu DM, Chen YJ, Chao MC, Chang TM, Lin JL, Chang CY, Kao YC, Lin SP. Lee CL, et al. Among authors: chen yj. Mol Genet Genomic Med. 2019 Aug;7(8):e790. doi: 10.1002/mgg3.790. Epub 2019 Jun 18. Mol Genet Genomic Med. 2019. PMID: 31215158 Free PMC article.

8

Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).

Chen CP, Chen YJ, Chern SR, Tsai FJ, Chang TY, Lee CC, Town DD, Lee MS, Wang W. Chen CP, et al. Among authors: chen yj. Prenat Diagn. 2008 May;28(5):450-3. doi: 10.1002/pd.1993. Prenat Diagn. 2008. PMID: 18395879 No abstract available.

9

Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.

Chen CP, Chen YJ, Chern SR, Tsai FJ, Lin HH, Lee CC, Wang W. Chen CP, et al. Among authors: chen yj. Prenat Diagn. 2008 Sep;28(9):865-7. doi: 10.1002/pd.2061. Prenat Diagn. 2008. PMID: 18661486 No abstract available.

10

NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).

Chen CP, Chen YJ, Tsai FJ, Chern SR, Wang W. Chen CP, et al. Among authors: chen yj. Prenat Diagn. 2008 Apr;28(4):364-5. doi: 10.1002/pd.1962. Prenat Diagn. 2008. PMID: 18383001 No abstract available.

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