Lin CC - Search Results

1

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

2

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. Chen CP, et al. Among authors: lin cc. Prenat Diagn. 2004 Oct;24(10):767-73. doi: 10.1002/pd.977. Prenat Diagn. 2004. PMID: 15503270 Review.

3

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W. Chen CP, et al. Among authors: lin sp, lin cc. Prenat Diagn. 2005 Feb;25(2):112-8. doi: 10.1002/pd.1083. Prenat Diagn. 2005. PMID: 15712324 Review.

4

Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.

Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W. Chen CP, et al. Among authors: lin cc. Prenat Diagn. 2006 Feb;26(2):138-46. doi: 10.1002/pd.1369. Prenat Diagn. 2006. PMID: 16470734 Review.

5

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).

Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W. Chen CP, et al. Among authors: lin cc. Prenat Diagn. 2006 Apr;26(4):313-20. doi: 10.1002/pd.1399. Prenat Diagn. 2006. PMID: 16506269 Review.

6

Genomic alterations in human malignant glioma cells associate with the cell resistance to the combination treatment with tumor necrosis factor-related apoptosis-inducing ligand and chemotherapy.

Li YC, Tzeng CC, Song JH, Tsia FJ, Hsieh LJ, Liao SJ, Tsai CH, Van Meir EG, Hao C, Lin CC. Li YC, et al. Among authors: lin cc. Clin Cancer Res. 2006 May 1;12(9):2716-29. doi: 10.1158/1078-0432.CCR-05-1980. Clin Cancer Res. 2006. PMID: 16675563

7

Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.

Chien SC, Chen CP, Lin CC, Huang LC, Hsieh CT, Tsai FJ. Chien SC, et al. Among authors: lin cc. Taiwan J Obstet Gynecol. 2009 Sep;48(3):292-5. doi: 10.1016/S1028-4559(09)60307-7. Taiwan J Obstet Gynecol. 2009. PMID: 19797023 Free article. Review.

8

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.

Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W. Chen CP, et al. Among authors: lin cc. Taiwan J Obstet Gynecol. 2010 Jun;49(2):188-91. doi: 10.1016/S1028-4559(10)60039-3. Taiwan J Obstet Gynecol. 2010. PMID: 20708526 Free article.

9

Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats.

Li YC, Chien SC, Setlur SR, Lin WD, Tsai FJ, Lin CC. Li YC, et al. Among authors: lin wd, lin cc. J Formos Med Assoc. 2015 Jan;114(1):81-7. doi: 10.1016/j.jfma.2011.05.015. Epub 2012 Mar 8. J Formos Med Assoc. 2015. PMID: 25618588 Free article. Review.

10

Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter).

Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Lee CC, Chen YJ, Wang W. Chen CP, et al. Among authors: lin sp, lin cc. Prenat Diagn. 2005 Aug;25(8):723-5. doi: 10.1002/pd.1223. Prenat Diagn. 2005. PMID: 16049995 No abstract available.

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