創辦人(TY)簡歷

Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis.

Chen CP, Su YN, Chang TY, Liu YP, Tsai FJ, Hwang JK, Wang W.

Taiwan J Obstet Gynecol. 2009 Sep;48(3):327-31.

Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites.

Chen CP, Tsai FJ, Chern SR, Chang TY, Hsu CY, Lin HH, Wang W.

Taiwan J Obstet Gynecol. 2009 Mar;48(1):84-7.

Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex.

Chen CP, Chang TY, Liu YP, Tsai FJ, Chien SC, Tsao CM, Yang HB, Wang W.

J Clin Ultrasound. 2008 Jun;36(5):308-11.

Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).

Chen CP, Chen YJ, Chern SR, Tsai FJ, Chang TY, Lee CC, Town DD, Lee MS, Wang W.

Prenat Diagn. 2008 May;28(5):450-3.

Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.

Chen CP, Chang TY, Lin HH, Chern SR, Wang W.

Taiwan J Obstet Gynecol. 2008 Mar;47(1):93-4.

Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidi, agenesis of the corpus callosum and mega cisterna magna.

Chen CP, Chang TY, Hung JH, Chen CY, Wang W.

Taiwan J Obstet Gynecol. 2008 Mar;47(1):91-2.

Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidney.

Chen CP, Liu YP, Huang JP, Chang TY, Tsai FJ, Tsai JD, Sheu JC, Wang W.

Ultrasound Obstet Gynecol. 2008 Mar;31(3):360-2.

Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly.

Chen CP, Lin SP, Chang TY, Ho HT.

Prenat Diagn. 2007 Dec;27(13):1266-7.

Third-trimester ultrasound evaluation of arachnoid cysts.

Chen CP, Chang TY, Wang W.

Taiwan J Obstet Gynecol. 2007 Dec;46(4):427-8.

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.

Prenat Diagn. 2007 Oct;27(10):967-9.

Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome.

Chen CP, Lin SP, Chang TY, Lee HC, Hung HY, Lin HY, Huang JP, Wang W.

J Clin Ultrasound. 2007 Sep;35(7):409-12.

Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.

Chen CP, Chang TY, Liu YP, Chern SR, Wang W.

Taiwan J Obstet Gynecol. 2007 Sep;46(3):284-5.

Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.

Chen CP, Chang TY, Chern SR, Wang W.

Taiwan J Obstet Gynecol. 2007 Sep;46(3):281-3.

Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.

Chen CP, Chang TY, Chern SR, Lee CC, Town DD, Lee MS, Wang W.

Prenat Diagn. 2007 Apr;27(4):383-5.

Early second-trimester diagnosis of fetal otocephaly.

Chen CP, Chang TY, Huang JK, Wang W.

Ultrasound Obstet Gynecol. 2007 Apr;29(4):470-1.

Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY).

Chen CP, Lin CJ, Chang TY, Chern SR, Tzen CY, Chen WL, Wang W.

Prenat Diagn. 2007 Mar;27(3):285-6.

Preliminary descriptive statistics of the Taiwanese Registry of Epilepsy and Pregnancy for the first 2 years.

Chang TY, Lai CW, Yu HY, Hsu JJ, Shih YH, Chen CP; Taiwanese Registry of Epilepsy and Pregnancy.

Taiwan J Obstet Gynecol. 2007 Mar;46(1):47-9.

Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis.

Chen CP, Lin CJ, Chang TY, Hsu CY, Tzen CY, Wang W.

Genet Couns. 2007;18(1):105-12.

Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).

Chen CP, Lin CC, Chang TY, Li YC, Hsieh LJ, Lee CC, Chen LF, Wang W.

Prenat Diagn. 2006 Aug;26(8):757-9.

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.

Prenat Diagn. 2006 Feb;26(2):184-5.

Prenatal two- and three-dimensional ultrasound diagnosis of limb reduction defects associated with homozygous alpha-thalassemia.

Chen CP, Chang TY, Su YN, Hsu CY, Wang W.

Fetal Diagn Ther. 2006;21(4):374-9.

Prenatal diagnosis of the supernumerary der(22)t(11;22) syndrome associated with abnormal sonographic findings.

Chen CP, Wang TH, Chang TY, Lee CC, Chen WL, Chen LF, Wang W.

Genet Couns. 2006;17(4):469-72.

Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings.

Chen CP, Lin SP, Chang TY, Tsai JD, Huang JK, Wang W.

Genet Couns. 2006;17(1):87-9.

Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).

Chen CP, Chern SR, Chang TY, Lee CC, Chen WL, Wang W.

Prenat Diagn. 2005 Nov;25(11):1069-71

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.

Prenat Diagn. 2005 Aug;25(8):721-3.

Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy.

Chen CP, Shih JC, Chang TY, Chern SR, Lin CY, Wang W, Tzen CY.

Prenat Diagn. 2005 Jul;25(7):618-20. No abstract available.

Prenatal magnetic resonance imaging of Galloway-Mowat syndrome.

Chen CP, Chang TY, Lin SP, Huang JK, Tsai JD, Chiu NC, Wang W.

Prenat Diagn. 2005 Jun;25(6):525-7.

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.

Prenat Diagn. 2005 Jun;25(6):523-4.

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.

Chen CP, Chern SR, Sheu JC, Lin SP, Hsu CY, Chang TY, Lee CC, Wang W, Chen HE.

Prenat Diagn. 2005 Jun;25(6):502-6.

Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.

Chen CP, Chern SR, Chang TY, Chen WL, Chen LF, Wang W, Cindy Chen HE.

Prenat Diagn. 2005 May;25(5):383-9.

Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).

Chen CP, Chang TY, Tzen CY, Wang W, Lee CC.

Prenat Diagn. 2005 Mar;25(3):263-4.

Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas.

Chen CP, Su YN, Hung CC, Lee CN, Hsieh FJ, Chang TY, Chen MR, Wang W.

Prenat Diagn. 2005 Feb;25(2):176-8.

Prenatal diagnosis of mosaic 22q11.2 microdeletion.

Chen CP, Chern SR, Lee CC, Lin SP, Chang TY, Wang W.

Prenat Diagn. 2004 Aug;24(8):660-2.

Prenatal sonographic diagnosis of acrania associated with amniotic bands.

Chen CP, Chang TY, Lin YH, Wang W.

J Clin Ultrasound. 2004 Jun;32(5):256-60.

Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature.

Chen CP, Chern SR, Cheng SJ, Chang TY, Yeh LF, Lee CC, Pan CW, Wang W, Tzen CY.

Prenat Diagn. 2004 Jun;24(6):455-62.

Second-trimester nasal bone hypoplasia/aplasia associated with cleidocranial dysplasia.

Chen CP, Hung HY, Chang TY, Lin SP, Wang W.

Prenat Diagn. 2004 May;24(5):399-400.

Prenatal identification of fetal overgrowth, abdominal wall defect, and neural tube defect in pregnancies achieved by assisted reproductive technology.

Chen CP, Lin SP, Hwu YM, Chang TY, Wang W.

Prenat Diagn. 2004 May;24(5):396-8.

Prenatal diagnosis of the distal 11q deletion and review of the literature.

Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.

Prenat Diagn. 2004 Feb;24(2):130-6.

Partial trisomy 10 (10q11.2-->pter) and partial trisomy 18 (18p11.2-->pter) associated with abnormal sonographic findings and a maternal serum screen-positive result.

Chen CP, Chang TY, Town DD, Chen LF, Pan CW, Wang W, Tzen CY.

Ultrasound Obstet Gynecol. 2004 Feb;23(2):202-4.

Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.

Chen CP, Lee CC, Chang TY, Town DD, Wang W.

Prenat Diagn. 2004 Jan;24(1):50-7.

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.

Chen CP, Chern SR, Lee CC, Chang TY, Wang W, Tzen CY.

Prenat Diagn. 2004 Jan;24(1):38-44.

Prenatal diagnosis of choledochal cyst using ultrasound and magnetic resonance imaging.

Chen CP, Cheng SJ, Chang TY, Yeh LF, Lin YH, Wang W.

Ultrasound Obstet Gynecol. 2004 Jan;23(1):93-4.

Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging.

Chen CP, Wang KG, Huang JK, Chang TY, Lin YH, Chin DT, Tzen CY, Wang W.

Ultrasound Obstet Gynecol. 2003 Aug;22(2):214-5.

Prenatal diagnosis of de novo terminal deletion of chromosome 7q.

Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Lee MS, Wang W.

Prenat Diagn. 2003 May;23(5):375-9.

Second-trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1-->qter.

Chen CP, Chang TY, Tzen CY, Wang W, Lee CC, Chen LF, Lee MS, Lin SP.

Ultrasound Obstet Gynecol. 2003 May;21(5):516-8.

Second-trimester sonographic detection of short rib-polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result.

Chen CP, Chang TY, Tzen CY, Wang W.

Prenat Diagn. 2003 Apr;23(4):353-5.

Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.

Chen CP, Chang TY, Chern SR, Town DD, Pan CW, Lee MS, Wang W.

Prenat Diagn. 2003 Apr;23(4):352-3.

Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomalies.

Chen CP, Tzen CY, Chang TY, Lin CJ, Wang W, Lee CC, Chen LF, Chen WL.

Ultrasound Obstet Gynecol. 2003 Feb;21(2):202-4.

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.

Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS.

Prenat Diagn. 2003 Jan;23(1):40-3.

Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly.

Chen CP, Tzen CY, Chang TY, Lin CJ, Wang W, Lee CC, Town DD, Chen LF, Lee MS.

Prenat Diagn. 2002 Dec;22(12):1112-3.

Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.

Chen CP, Chang TY, Shih JC, Lin SP, Lin CJ, Wang W, Lee CC, Town DD, Pan CW, Tzen CY.

Prenat Diagn. 2002 Dec;22(12):1063-6.

Perinatal imaging findings of inherited Sotos syndrome.

Chen CP, Lin SP, Chang TY, Chiu NC, Shih SL, Lin CJ, Wang W, Hsu HC.

Prenat Diagn. 2002 Oct;22(10):887-92.

Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.

Chen CP, Chern SR, Chang TY, Lin CJ, Wang W, Tzen CY.

Prenat Diagn. 2002 Aug;22(8):736-7.

Prenatal diagnosis of acrania associated with facial defects, amniotic bands and limb-body wall complex.

Chen CP, Tzen CY, Chang TY, Yeh LF, Wang W.

Ultrasound Obstet Gynecol. 2002 Jul;20(1):94-5.

Sonographic detection of situs inversus, ventricular septal defect, and short-rib polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus not known to be at risk.

Chen CP, Chang TY, Tzen CY, Lin CJ, Wang W.

Ultrasound Obstet Gynecol. 2002 Jun;19(6):629-31.

Sonographic appearance of the uterus after simple square suturing for rapid control of postpartum hemorrhage and preservation of fertility.

Chen CP, Chang TY, Yeh LF, Lin CJ, Wang W.

J Clin Ultrasound. 2002 Mar-Apr;30(3):189-91.

Fetal cervico-mediastinal cystic hygroma associated with maternal serum screening positive for Down syndrome.

Chen CP, Sheu JC, Wang W, Lin SP, Chang TY, Tzen CY.

Prenat Diagn. 2002 Feb;22(2):166.

Resolution of fetal bilateral chylothorax and ascites after two unilateral thoracocenteses.

Chen CP, Chang TY, Wang W.

Ultrasound Obstet Gynecol. 2001 Oct;18(4):401-2.

Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.

Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.

Prenat Diagn. 2001 May;21(5):346-50.

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.

Chen CP, Chern SR, Tzen CY, Lee MS, Pan CW, Chang TY, Wang W.

Prenat Diagn. 2001 Apr;21(4):317-20.

Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia.

Chen CP, Chern SR, Shih JC, Wang W, Yeh LF, Chang TY, Tzen CY.

Prenat Diagn. 2001 Feb;21(2):89-95.