Hung FY - Search Results

1

Prenatal diagnosis of pure distal 18q deletion.

Chen CP, Chern SR, Hung FY, Hsu CY, Chang TY, Lee CC, Town DD, Chen WL, Chen LF, Tzen CY, Wang W, Ma R. Chen CP, et al. Among authors: hung fy. Prenat Diagn. 2006 Feb;26(2):184-5. doi: 10.1002/pd.1367. Prenat Diagn. 2006. PMID: 16470512 No abstract available.

2

Placenta percreta presenting as a pinhole uterine rupture and acute abdomen.

Hung FY, Wang PT, Weng SL, Chen CP. Hung FY, et al. Taiwan J Obstet Gynecol. 2010 Mar;49(1):115-6. doi: 10.1016/S1028-4559(10)60024-1. Taiwan J Obstet Gynecol. 2010. PMID: 20466308 Free article. No abstract available.

3

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.

Chen CP, Su YN, Lin SY, Chang CL, Wang YL, Huang JP, Chen CY, Hung FY, Chen YY, Wu PC, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2011 Mar;50(1):85-94. doi: 10.1016/j.tjog.2010.05.001. Taiwan J Obstet Gynecol. 2011. PMID: 21482381 Free article.

4

Prenatal diagnosis of mosaic trisomy 9.

Chen CP, Hung FY, Su YN, Chern SR, Su JW, Lee CC, Chen YT, Chen WL, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2011 Dec;50(4):549-53. doi: 10.1016/j.tjog.2011.10.031. Taiwan J Obstet Gynecol. 2011. PMID: 22212338 Free article. No abstract available.

5

Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II.

Chen CP, Su YN, Hung FY, Chern SR, Su JW, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2012 Jun;51(2):312-4. doi: 10.1016/j.tjog.2012.04.031. Taiwan J Obstet Gynecol. 2012. PMID: 22795120 Free article. No abstract available.

6

Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony.

Chen CP, Hung FY, Chern SR, Wu PS, Su JW, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2013 Jun;52(2):300-2. doi: 10.1016/j.tjog.2013.04.031. Taiwan J Obstet Gynecol. 2013. PMID: 23915872 Free article. No abstract available.

7

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee MS, Yang CW, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2016 Dec;55(6):902-903. doi: 10.1016/j.tjog.2016.10.001. Taiwan J Obstet Gynecol. 2016. PMID: 28040147 Free article. No abstract available.

8

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

Chen CP, Chen M, Chang SP, Hung FY, Lee MJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Chen WL, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2017 Apr;56(2):234-237. doi: 10.1016/j.tjog.2017.01.004. Taiwan J Obstet Gynecol. 2017. PMID: 28420515 Free article.

9

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2017 Apr;56(2):268-269. doi: 10.1016/j.tjog.2017.01.007. Taiwan J Obstet Gynecol. 2017. PMID: 28420524 Free article. No abstract available.

10

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Chen CP, Chang TY, Hung FY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Lee CC, Wang W. Chen CP, et al. Among authors: hung fy. Taiwan J Obstet Gynecol. 2017 Dec;56(6):843-846. doi: 10.1016/j.tjog.2017.10.026. Taiwan J Obstet Gynecol. 2017. PMID: 29241932 Free article.

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