Liu YP - Search Results

1

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: liu yp. Prenat Diagn. 2007 Oct;27(10):967-9. doi: 10.1002/pd.1797. Prenat Diagn. 2007. PMID: 17602449 No abstract available.

2

Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.

Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W. Chen CP, et al. Among authors: liu yp. Taiwan J Obstet Gynecol. 2011 Sep;50(3):345-52. doi: 10.1016/j.tjog.2011.07.014. Taiwan J Obstet Gynecol. 2011. PMID: 22030051 Free article.

3

Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).

Chen CP, Lin YH, Au HK, Su YN, Hsu CY, Liu YP, Wu PC, Chern SR, Chen YT, Chen LF, Hsieh AH, Wang W. Chen CP, et al. Among authors: liu yp. Taiwan J Obstet Gynecol. 2011 Sep;50(3):359-65. doi: 10.1016/j.tjog.2011.07.004. Taiwan J Obstet Gynecol. 2011. PMID: 22030053 Free article.

4

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.

Chen CP, Lin CJ, Chern SR, Liu YP, Kuo YL, Chen YN, Wu PS, Town DD, Chen LF, Yang CW, Wang W. Chen CP, et al. Among authors: liu yp. Taiwan J Obstet Gynecol. 2014 Dec;53(4):583-7. doi: 10.1016/j.tjog.2014.10.002. Taiwan J Obstet Gynecol. 2014. PMID: 25510705 Free article.

5

Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.

Chen CP, Lin SP, Chen M, Su YN, Chern SR, Wang TY, Liu YP, Tsai FJ, Lee CC, Chen YJ, Wang W. Chen CP, et al. Among authors: liu yp. Genet Couns. 2011;22(3):273-80. Genet Couns. 2011. PMID: 22029168

6

Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.

Chen CP, Lin SP, Chen MR, Su YN, Chern SR, Liu YP, Su JW, Lee MS, Wang W. Chen CP, et al. Among authors: liu yp. Genet Couns. 2012;23(3):405-13. Genet Couns. 2012. PMID: 23072190

7

Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas.

Chen CP, Liu YP, Huang JK, Chang TY, Chen MR, Chiu NC, Wang W. Chen CP, et al. Among authors: liu yp. Prenat Diagn. 2005 Jun;25(6):523-4. doi: 10.1002/pd.1182. Prenat Diagn. 2005. PMID: 15966047 No abstract available.

8

Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression.

Chen CP, Liu YP, Lin SP, Sheu JC, Hsu CY, Chang TY, Wang W. Chen CP, et al. Among authors: liu yp. Prenat Diagn. 2005 Aug;25(8):721-3. doi: 10.1002/pd.1209. Prenat Diagn. 2005. PMID: 16049993 No abstract available.

9

Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst.

Chen CP, Liu YP, Hsu CY, Lin SP, Wang W. Chen CP, et al. Among authors: liu yp. Prenat Diagn. 2006 May;26(5):489-91. doi: 10.1002/pd.1452. Prenat Diagn. 2006. PMID: 16652397 No abstract available.

10

Congenital cystic adenomatoid malformation in twin-twin transfusion syndrome: fetal MR imaging.

Liu YP, Chang TY. Liu YP, et al. Pediatr Radiol. 2007 Sep;37(9):941. doi: 10.1007/s00247-007-0530-1. Epub 2007 Jun 26. Pediatr Radiol. 2007. PMID: 17593361 No abstract available.

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