Wu PC - Search Results

1

A call for a standardized placenta accreta spectrum screening in Taiwan.

Wu PC, Olisova K, Ko H, Chang TY. Wu PC, et al. Taiwan J Obstet Gynecol. 2023 Jan;62(1):191-192. doi: 10.1016/j.tjog.2022.11.004. Taiwan J Obstet Gynecol. 2023. PMID: 36720543 Free article. No abstract available.

2

Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene.

Chen CP, Chang TY, Chen CY, Wang TY, Tsai FJ, Wu PC, Chern SR, Wang W. Chen CP, et al. Among authors: wu pc. Taiwan J Obstet Gynecol. 2012 Mar;51(1):100-5. doi: 10.1016/j.tjog.2012.01.020. Taiwan J Obstet Gynecol. 2012. PMID: 22482978 Free article.

3

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.

Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W. Chen CP, et al. Among authors: wu pc, wu ps. Taiwan J Obstet Gynecol. 2014 Mar;53(1):90-4. doi: 10.1016/j.tjog.2013.12.003. Taiwan J Obstet Gynecol. 2014. PMID: 24767654 Free article.

4

Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.

Chen YN, Chen CP, Ko TM, Wang LK, Wu PC, Chang TY, Wu PS, Yang CW, Wang W. Chen YN, et al. Among authors: wu pc, wu ps. Taiwan J Obstet Gynecol. 2016 Feb;55(1):117-20. doi: 10.1016/j.tjog.2015.12.014. Taiwan J Obstet Gynecol. 2016. PMID: 26927262 Free article.

5

Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.

Chen CP, Wang LK, Wu PC, Chang TY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W. Chen CP, et al. Among authors: wu pc, wu ps. Taiwan J Obstet Gynecol. 2017 Feb;56(1):102-105. doi: 10.1016/j.tjog.2016.12.004. Taiwan J Obstet Gynecol. 2017. PMID: 28254208 Free article.

6

Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy.

Chen CP, Liu YP, Chang TY, Tsai FJ, Chen CY, Wu PC, Chen TH, Wang W. Chen CP, et al. Among authors: wu pc. Taiwan J Obstet Gynecol. 2010 Sep;49(3):385-6. doi: 10.1016/S1028-4559(10)60082-4. Taiwan J Obstet Gynecol. 2010. PMID: 21056332 Free article. No abstract available.

7

Prenatal Diagnosis of Persistent Left Superior Vena Cava is Associated with Coarctation of the Aorta - A Case Report.

Wen TM, Huang YL, Wu PC, Li YY, Chen MR, Chang TY. Wen TM, et al. Among authors: wu pc. J Med Ultrasound. 2017 Oct-Dec;25(4):244-247. doi: 10.1016/j.jmu.2017.05.003. Epub 2017 Oct 10. J Med Ultrasound. 2017. PMID: 30065501 Free PMC article.

8

Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings.

Chen CP, Chang TY, Hsu CY, Liu YP, Tsai FJ, Wu PC, Wang W. Chen CP, et al. Among authors: wu pc. J Chin Med Assoc. 2012 Apr;75(4):190-3. doi: 10.1016/j.jcma.2012.02.007. Epub 2012 Mar 23. J Chin Med Assoc. 2012. PMID: 22541150 Free article.

9

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.

Chen CP, Chang TY, Guo WY, Wu PC, Wang LK, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. Chen CP, et al. Among authors: wu pc, wu ps. Gene. 2013 Dec 10;532(1):152-9. doi: 10.1016/j.gene.2013.09.044. Epub 2013 Sep 19. Gene. 2013. PMID: 24055730 Review.

10

Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3.

Chen SW, Chen CP, Wang LK, Chern SR, Wu PC, Chen YN, Lin CJ, Chen WL, Wang W. Chen SW, et al. Among authors: wu pc. Taiwan J Obstet Gynecol. 2017 Feb;56(1):87-92. doi: 10.1016/j.tjog.2016.12.013. Taiwan J Obstet Gynecol. 2017. PMID: 28254233 Free article.

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