Li YC - Search Results

1

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. 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.

2

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. Among authors: li yc. Prenat Diagn. 2006 Oct;26(10):898-902. doi: 10.1002/pd.1520. Prenat Diagn. 2006. PMID: 16915592

3

Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX male.

Chien SC, Li YC, Ho M, Hsu PC, Teng RH, Lin WD, Tsai FJ, Lin CC. Chien SC, et al. Among authors: li yc. Am J Med Genet A. 2009 Dec;149A(12):2775-81. doi: 10.1002/ajmg.a.32958. Am J Med Genet A. 2009. PMID: 19921641

4

A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate.

Chien SC, Li YC, Li LH, Wu JY, Hsu PC, Shi SL, Tsai FJ, Lin CC. Chien SC, et al. Among authors: li lh, li yc. Am J Med Genet A. 2010 Jul;152A(7):1862-7. doi: 10.1002/ajmg.a.33452. Am J Med Genet A. 2010. PMID: 20583161 No abstract available.

5

Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.

Sung PL, Chang CM, Chen CY, Wang PH, Chao KC, Wen KC, Cheng YY, Li YC, Lin CC. Sung PL, et al. Among authors: li yc. Taiwan J Obstet Gynecol. 2012 Jun;51(2):260-5. doi: 10.1016/j.tjog.2012.04.017. Taiwan J Obstet Gynecol. 2012. PMID: 22795105 Free article.

6

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: li yc. Prenat Diagn. 2004 Oct;24(10):767-73. doi: 10.1002/pd.977. Prenat Diagn. 2004. PMID: 15503270 Review.

7

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: li yc. Prenat Diagn. 2005 Feb;25(2):112-8. doi: 10.1002/pd.1083. Prenat Diagn. 2005. PMID: 15712324 Review.

8

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: li yc. Prenat Diagn. 2006 Feb;26(2):138-46. doi: 10.1002/pd.1369. Prenat Diagn. 2006. PMID: 16470734 Review.

9

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: li yc. Prenat Diagn. 2006 Apr;26(4):313-20. doi: 10.1002/pd.1399. Prenat Diagn. 2006. PMID: 16506269 Review.

10

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype.

Sung PL, Chang SP, Wen KC, Chang CM, Yang MJ, Chen LC, Chao KC, Huang CY, Li YC, Lin CC. Sung PL, et al. Among authors: li yc. Am J Med Genet A. 2009 Dec;149A(12):2768-74. doi: 10.1002/ajmg.a.32878. Am J Med Genet A. 2009. PMID: 19921638

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