Chih-Ping Chen

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TOP 3
Chen Chih-Ping; Liu Yu-Peng; Tsai Fuu-Jen; Chen Chen-Yu; Lin Hung-Hung; Wu Pei-Chen; Wang Wayseen
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review.
Chen Chih-Ping
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (II).
Chen Chih-Ping
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I).

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All Publications

2009: Chen Chih-Ping; Liu Yu-Peng; Tsai Fuu-Jen; Chen Chen-Yu; Lin Hung-Hung; Wu Pei-Chen; Wang Wayseen
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review.
Taiwanese journal of obstetrics & gynecology 2009;48(3):286-91.
2009: Chen Chih-Ping
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (II).
Taiwanese journal of obstetrics & gynecology 2009;48(3):218-24.
2009: Chen Chih-Ping
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I).
Taiwanese journal of obstetrics & gynecology 2009;48(3):210-7.
2009: Liu Yu-Peng; Chen Chih-Ping
Fetal MRI of hydrometrocolpos with septate vagina and uterus didelphys as well as massive urinary ascites due to cloacal malformation.
Pediatric radiology 2009;39(8):877.
2009: Chen Chih-Ping
Placental abnormalities and preeclampsia in trisomy 13 pregnancies.
Taiwanese journal of obstetrics & gynecology 2009;48(1):3-8.
2008: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Wang Tzu-Hao; Chern Schu-Rern; Wang Wayseen
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
Fertility and sterility 2008;90(4):1198.e11-8.
2008: Chen Chih-Ping
Prenatal diagnosis, fetal surgery, recurrence risk and differential diagnosis of neural tube defects.
Taiwanese journal of obstetrics & gynecology 2008;47(3):283-90.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (VII).
Taiwanese journal of obstetrics & gynecology 2008;47(3):276-82.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (VI).
Taiwanese journal of obstetrics & gynecology 2008;47(3):267-75.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (V).
Taiwanese journal of obstetrics & gynecology 2008;47(3):259-66.
2008: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.
European journal of medical genetics 2008;51(4):368-72.
2008: Wu Hong-Ming; Chen Chih-Ping; Chang Kuo-Ming; Chang Shing-Jyh
Omental trophoblastic implant with hemoperitoneum as a sequela of suction dilatation and curettage.
Taiwanese journal of obstetrics & gynecology 2008;47(2):250-1.
2008: Chen Shwu-Shiuang; Chen Chih-Ping; Chien Shu-Chin; Hsu Chin-Yuan
Spontaneous rupture of omental teratoma mimicking a ruptured ovarian teratoma.
Taiwanese journal of obstetrics & gynecology 2008;47(2):229-32.
2008: Peng Yu-Yueh; Chen Chih-Ping; Chien Shu-Chin; Chen Jen-Ruei
Torsion of a huge ovarian cyst in a 90-year-old woman.
Taiwanese journal of obstetrics & gynecology 2008;47(2):224-5.
2008: Hsu Kuang-Pin; Chen Chih-Ping; Chien Shu-Chin; Hsu Chin-Yuan
Hematocolpometra associated with an imperforate hymen and acute urinary retention mimicking a pelvic mass.
Taiwanese journal of obstetrics & gynecology 2008;47(2):222-3.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (IV).
Taiwanese journal of obstetrics & gynecology 2008;47(2):141-50.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (III).
Taiwanese journal of obstetrics & gynecology 2008;47(2):131-40.
2008: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Wang Wayseen
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
Fertility and sterility 2008;89(6):1826.e5-7.
2008: Chen Chih-Ping; Chang Tung-Yao; Liu Yu-Peng; Tsai Fuu-Jen; Chien Shu-Chin; Tsao Chien-Ming; Yang Hsiao-Bai; Wang Wayseen
Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex.
Journal of clinical ultrasound : JCU 2008;36(5):308-11.
2008: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Chang Tung-Yao; Lee Chen-Chi; Town Dai-Dyi; Lee Meng-Shan; Wang Wayseen
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).
Prenatal diagnosis 2008;28(5):450-3.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (II).
Taiwanese journal of obstetrics & gynecology 2008;47(1):10-7.
2008: Chen Chih-Ping
Syndromes, disorders and maternal risk factors associated with neural tube defects (I).
Taiwanese journal of obstetrics & gynecology 2008;47(1):1-9.
2008: Chen C-P; Lin S-P; Su Y-N; Chien S-C; Tsai F-J; Wang W
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
Genetic counseling (Geneva, Switzerland) 2008;19(2):165-72.
2007: Chen Yu-Wei; Yang Yuh-Cheng; Chen Chih-Ping; Chen Han-Hsiang; Chen Yi-Chou; Yeh Jui-Chi; Wu Chih-Jen
Concomitant Serratia marcescens peritonitis and tubo-ovarian abscess associated with peritoneal dialysis and intrauterine device placement.
Taiwanese journal of obstetrics & gynecology 2007;46(4):429-30.
2007: Chen Chih-Ping
Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy.
Taiwanese journal of obstetrics & gynecology 2007;46(4):336-51.
2007: Chen Chih-Ping
Chromosomal abnormalities associated with neural tube defects (I): full aneuploidy.
Taiwanese journal of obstetrics & gynecology 2007;46(4):325-35.
2007: Chen Chih-Ping; Lin Shuan-Pei; Chang Tung-Yao; Ho Hsin-Tsung
Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly.
Prenatal diagnosis 2007;27(13):1266-7.
2007: Chen Chih-Ping; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p.
Prenatal diagnosis 2007;27(12):1170-3.
2007: Chen Chih-Ping; Wang Tzu-Hao; Chen Yann-Jang; Chang Tung-Yao; Liu Yu-Peng; Tzen Chin-Yuan; Chern Schu-Rern; Wang Wayseen
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.
Prenatal diagnosis 2007;27(10):967-9.
2007: Chen Chih-Ping
Prenatal diagnosis of iniencephaly.
Taiwanese journal of obstetrics & gynecology 2007;46(3):199-208.
2007: Chen Chih-Ping
Prenatal diagnosis of arachnoid cysts.
Taiwanese journal of obstetrics & gynecology 2007;46(3):187-98.
2007: Chen Chih-Ping; Lin Shuan-Pei; Chang Tung-Yao; Lee Hung-Chang; Hung Han-Yang; Lin Hsiang-Yu; Huang Jian-Pei; Wang Wayseen
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome.
Journal of clinical ultrasound : JCU 2007;35(7):409-12.
2007: Huang Ming-Chao; Chen Chih-Ping; Su Tsung-Hsien; Wang Kung-Liahng; Yang Yuh-Cheng; Hwu Yuh-Ming
The safety and efficacy of microwave endometrial ablation after endometrial curettage without hormonal pretreatment.
Taiwanese journal of obstetrics & gynecology 2007;46(2):152-6.
2007: Chen Chih-Ping
Syndromes and disorders associated with omphalocele (III): single gene disorders, neural tube defects, diaphragmatic defects and others.
Taiwanese journal of obstetrics & gynecology 2007;46(2):111-20.
2007: Chen Chih-Ping
Syndromes and disorders associated with omphalocele (II): OEIS complex and Pentalogy of Cantrell.
Taiwanese journal of obstetrics & gynecology 2007;46(2):103-10.
2007: Chen Chih-Ping
Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome.
Taiwanese journal of obstetrics & gynecology 2007;46(2):96-102.
2007: Chang Tung-Yao; Lai Chi-Wan; Yu Hsiang-Yu; Hsu Jenn-Jeih; Shih Yang-Hsin; Chen Chih-Ping;
Preliminary descriptive statistics of the Taiwanese Registry of Epilepsy and Pregnancy for the first 2 years.
Taiwanese journal of obstetrics & gynecology 2007;46(1):47-9.
2007: Chen Chih-Ping
Meckel syndrome: genetics, perinatal findings, and differential diagnosis.
Taiwanese journal of obstetrics & gynecology 2007;46(1):9-14.
2007: Chen Chih-Ping
Chromosomal abnormalities associated with omphalocele.
Taiwanese journal of obstetrics & gynecology 2007;46(1):1-8.
2007: Chen C P; Chien S C; Chern S R; Tzen C Y; Wang W
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies.
Genetic counseling (Geneva, Switzerland) 2007;18(3):343-7.
2007: Liu Chien-Liang; Chang Yuan-Ching; Cheng Shih-Ping; Chern Schu-Rern; Yang Tsen-Long; Lee Jie-Jen; Guo Ing-Cherng; Chen Chih-Ping
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer.
Oncology 2007;72(1-2):75-81.
2007: Chen C P; Lin C J; Chang T Y; Hsu C Y; Tzen C Y; Wang W
Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis.
Genetic counseling (Geneva, Switzerland) 2007;18(1):105-12.
2007: Chen C P; Lin S P; Tzen C Y; Hwu W L; Chern S R; Chuang C K; Chiang S S; Wang W
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
Genetic counseling (Geneva, Switzerland) 2007;18(1):49-56.
2006: Cheng Hung-Pin; Hsu Chin-Yuan; Chen Chih-Ping; Su Tsung-Hsien
Angiomyxoma of the umbilical cord.
Taiwanese journal of obstetrics & gynecology 2006;45(4):360-2.
2006: Wu Chia-Fang; Hsu Chin-Yuan; Chen Chih-Ping
Ectopic molar pregnancy in a cesarean scar.
Taiwanese journal of obstetrics & gynecology 2006;45(4):343-5.
2006: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Wang Wayseen
Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Fertility and sterility 2006;86(5):1514.e1-2.
2006: Chen C-P; Wang T-H; Lin S-P; Chern S-R; Chen M-R; Lee C-C; Chen Y-J; Wang W
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
European journal of medical genetics 2006;49(6):516-9.
2006: Huang Yu-Hui; Hsu Chin-Yuan; Chang Yi-Fang; Chen Chih-Ping
Postcesarean splenic torsion.
Taiwanese journal of obstetrics & gynecology 2006;45(3):257-9.
2006: Chen Chih-Ping; Lin Shuan-Pei; Wang Tzu-Hao; Chen Yann-Jang; Chen Ming; Wang Wayseen
Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.
Prenatal diagnosis 2006;26(8):725-9.
2006: Chen Chih-Ping; Su Yi-Ning; Hung Chia-Cheng; Shih Jin-Chung; Wang Wayseen
Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis.
Journal of the Formosan Medical Association = Taiwan yi zhi 2006;105(7):599-603.
2006: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Chen Yann-Jang; Chern Schu-Rern; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.
American journal of medical genetics. Part A 2006;140(14):1594-600.
2006: Wong Chiong-Hee; Chen Tien-Ling; Lee Chyou-Shen; Lin Chen-Ju; Chen Chih-Ping
Outcome of pregnancy in patients with systemic lupus erythematosus.
Taiwanese journal of obstetrics & gynecology 2006;45(2):120-3.
2006: Chen Chih-Ping; Chern Schu-Rern; Lin Chyi-Chyang; Wang Tzu-Hao; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Hua Hui-Min; Wang Wayseen
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Prenatal diagnosis 2006;26(4):313-20.
2006: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Chen Wen-Lin; Wang Wayseen
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.
Prenatal diagnosis 2006;26(2):138-46.
2006: Chen C P; Lin S P; Lee C C; Town D D; Wang W
Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
Genetic counseling (Geneva, Switzerland) 2006;17(3):301-6.
2006: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2006: Chen Chih-Ping; Chang Tung-Yao; Su Yi-Ning; Hsu Chin-Yuan; Wang Wayseen
Prenatal two- and three-dimensional ultrasound diagnosis of limb reduction defects associated with homozygous alpha-thalassemia.
Fetal diagnosis and therapy 2006;21(4):374-9.
2006: Chen C P; Lee C C; Town D D; Chen W L; Chen L F; Lee M S; Pan C W; Wang W
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis.
Genetic counseling (Geneva, Switzerland) 2006;17(1):91-5.
2006: Chen C P; Lin S P; Lin C C; Li Y C; Hsieh L J; Huang J K; Lee C C; Wang W
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Genetic counseling (Geneva, Switzerland) 2006;17(1):57-63.
2005: Chen Chih-Ping; Chern Schu-Rern; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Wang Tzu-Hao; Lee Chen-Chi; Pan Chen-Wen; Hsieh Lie-Jiau; Wang Wayseen
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.
American journal of medical genetics. Part A 2005;139A(2):146-50.
2005: Lin Yi-Hui; Chen Chih-Ping; Chiang Sheng; Chen Tze-Chien
Ovarian abscess caused by nontyphoidal Salmonella in a woman with systemic lupus erythematosus: a case report.
The Journal of reproductive medicine 2005;50(8):627-9.
2005: Chen Chih-Ping; Shih Jin-Chung; Hsu Chin-Yuan; Chen Chen-Yu; Huang Jon-Kway; Wang Wayseen
Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly.
Journal of clinical ultrasound : JCU 2005;33(6):312-8.
2005: Chen Chih-Ping; Cheng Sho-Jen; Lin Yi-Hui; Wang Wayseen
Prenatal imaging of limb-body wall complex by magnetic resonance imaging.
Prenatal diagnosis 2005;25(6):521-3.
2005: Chen Chih-Ping; Chern Schu-Rern; Sheu Jin-Chern; Lin Shuan-Pei; Hsu Chin-Yuan; Chang Tung-Yao; Lee Chen-Chi; Wang Wayseen; Chen Hsiao-En Cindy
Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
Prenatal diagnosis 2005;25(6):502-6.
2005: Chen Chih-Ping; Chern Schu-Rern; Wang Tzu-Hao; Hsueh Ding-Wei; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen; Ko Tsang-Ming
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Prenatal diagnosis 2005;25(6):492-6.
2005: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen; Cindy Chen Hsiao-En
Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.
Prenatal diagnosis 2005;25(5):383-9.
2005: Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Lin Ching-Yi; Lin Yi-Hui; Wang Wayseen
A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.
Prenatal diagnosis 2005;25(4):327-30.
2005: Chen Chih-Ping; Chang Tung-Yao; Tzen Chin-Yuan; Wang Wayseen; Lee Chen-Chi
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
Prenatal diagnosis 2005;25(3):263-4.
2005: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Chen Wei-Min; Lee Chen-Chi; Hsieh Lie-Jiau; Wang Wayseen
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Prenatal diagnosis 2005;25(2):112-8.
2005: Chen Hui-Ju; Lin Shuan-Pei; Lee Hung-Chang; Chen Chih-Ping; Chiu Nan-Chang; Hung Han-Yang; Chern Schu-Rern; Chuang Chih-Kuang
Cystic fibrosis with homozygous R553X mutation in a Taiwanese child.
Journal of human genetics 2005;50(12):674-8.
2005: Chen C P
Fetal therapy and cytogenetic testing: prenatal detection of chromosome aberration during thoracocentesis for congenital chylothorax by karyotyping from pleural effusion fluid and review of the literature.
Genetic counseling (Geneva, Switzerland) 2005;16(3):301-5.
2005: Chen C P; Chern S R; Lin C J; Lee C C; Wang W; Tzen C Y
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly.
Genetic counseling (Geneva, Switzerland) 2005;16(1):49-57.
2004: Chen Chih-Ping; Cheng Sho-Jen; Sheu Jin-Chern; Lin Yi-Hui
Third-trimester evaluation of choledochal cyst using magnetic resonance imaging.
Prenatal diagnosis 2004;24(10):838-9.
2004: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Lee Men-Shan; Wang Wayseen; Tzen Chin-Yuan
Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
Prenatal diagnosis 2004;24(10):767-73.
2004: Chen Chih-Ping; Chern Schu-Rern; Cheng Sho-Jen; Chang Tung-Yao; Yeh Li-Fan; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen; Tzen Chin-Yuan
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.
Prenatal diagnosis 2004;24(6):455-62.
2004: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chen Chih-Ping; Chang Tung-Yao; Lin Yi-Hui; Wang Wayseen
Prenatal sonographic diagnosis of acrania associated with amniotic bands.
Journal of clinical ultrasound : JCU 2004;32(5):256-60.
2004: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chen C-P; Chang T-Y; Town D-D; Chen L-F; Pan C-W; Wang W; Tzen C-Y
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.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2004;23(2):202-4.
2004: Chen C-P; Cheng S-J; Chang T-Y; Yeh L-F; Lin Y-H; Wang W
Prenatal diagnosis of choledochal cyst using ultrasound and magnetic resonance imaging.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2004;23(1):93-4.
2004: Chen Chih-Ping; Shih Jin-Chung; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
Prenatal diagnosis 2004;24(1):63-6.
2004: Chen Chih-Ping; Lee Chen-Chi; Chang Tung-Yao; Town Dai-Dyi; Wang Wayseen
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Prenatal diagnosis 2004;24(1):50-7.
2004: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chang Tung-Yao; Wang Wayseen; Tzen Chin-Yuan
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2004: Chen Chih-Ping; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen; Tzen Chin-Yuan
Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
Prenatal diagnosis 2004;24(1):19-25.
2004: Chen C P; Lee C C; Town D D; Lee M S; Wang W
Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
Genetic counseling (Geneva, Switzerland) 2004;15(4):473-6.
2004: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W; Liao Y W
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Genetic counseling (Geneva, Switzerland) 2004;15(4):437-42.
2003: Chen Chih-Ping; Chern Schu-Rern; Town Dai-Dyi; Wang Wayseen; Liao You-Wei
Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
Prenatal diagnosis 2003;23(12):1019-21.
2003: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Li-Feng; Chin Daniel T H; Tzen Chin-Yuan; Wang Wayseen
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chen C-P; Shih J-C; Shih S-L; Huang J-K; Huang J-P; Lin Y-H; Wang W
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2003;22(3):299-304.
2003: Chen Chih-Ping; Lin Shuan-Pei; Chern Schu-Rern; Shih Shin-Lin; Lee Chen-Chi; Wang Wayseen; Liao You-Wei
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chen Chih-Ping; Hwu Yuh-Ming; Yeh Li-Fan; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.
Fertility and sterility 2003;79(5):1231-3.
2003: Chen Chih-Ping; Chang Tung-Yao; Chern Schu-Rern; Town Dai-Dyi; Pan Chen-Wen; Lee Meng-Shan; Wang Wayseen
Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.
Prenatal diagnosis 2003;23(4):352-3.
2003: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Lee Chen-Chi; Chen Li-Feng; Tzen Chin-Yuan; Wang Wayseen; Lin Chen-Ju; Yang Brian P T; Yang Lawrence S T
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2003: Chen C P; Lin S P
Distal 10q trisomy associated with bilateral hydronephrosis in infancy.
Genetic counseling (Geneva, Switzerland) 2003;14(3):359-62.
2002: Chen Chih-Ping; Chang Tung-Yao; Shih Jin-Chung; Lin Shuan-Pei; Lin Chen-Ju; Wang Wayseen; Lee Chen-Chi; Town Dai-Dyi; Pan Chen-Wen; Tzen Chin-Yuan
Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Prenatal diagnosis 2002;22(12):1063-6.
2002: Chen Chih-Ping; Lin Shuan-Pei; Chang Tung-Yao; Chiu Nan-Chang; Shih Shin-Lin; Lin Chen-Ju; Wang Wayseen; Hsu Hong-Chih
Perinatal imaging findings of inherited Sotos syndrome.
Prenatal diagnosis 2002;22(10):887-92.
2002: Chen C P; Tzen C Y; Chang T Y; Yeh L F; Wang W
Prenatal diagnosis of acrania associated with facial defects, amniotic bands and limb-body wall complex.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2002;20(1):94-5.
2002: Chen Chih-Ping; Yang Yuh-Cheng; Lin Shuan-Pei; Wang Wayseen; Chang Chih-Long; Chang Kuo-Ming
Bilateral calcified ovarian fibromas in a patient with Sotos syndrome.
Fertility and sterility 2002;77(6):1285-7.
2002: Chen Chih-Ping; Chang Tung-Yao; Yeh Li-Fan; Lin Chen-Ju; Wang Wayseen
Sonographic appearance of the uterus after simple square suturing for rapid control of postpartum hemorrhage and preservation of fertility.
Journal of clinical ultrasound : JCU 2002;30(3):189-91.
2002: Chen Chih-Ping; Chern Schu-Rern; Du Shin-Hua; Wang Wayseen
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2002;22(1):5-7.
2001: Chen H H; Lin H C; Yeh J C; Chen C P
Renal biopsy in pregnancies complicated by undetermined renal disease.
Acta obstetricia et gynecologica Scandinavica 2001;80(10):888-93.
2001: Chen C P; Chern S R; Wang W; Lee C C; Chen W L; Chen L F; Chang T Y; Tzen C Y
Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2001;21(5):346-50.
2001: Chen C P; Chern S R; Tzen C Y; Lee M S; Pan C W; Chang T Y; Wang W
Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.
Prenatal diagnosis 2001;21(4):317-20.
2001: Chen C P; Chern S R; Wang W; Wang K L; Wang T Y
Multiple globules in a cystic ovarian teratoma.
Fertility and sterility 2001;75(3):618-9.
2001: Chen C P; Chern S R; Lee C C; Chen W L; Wang W
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2001: Chen C P; Chern S R; Shih J C; Wang W; Yeh L F; Chang T Y; Tzen C Y
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia.
Prenatal diagnosis 2001;21(2):89-95.
2000: Chen C P; Chern S R; Chang C L; Lee C C; Chen W L; Chen L F; Wang W
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chen C P; Chern S R; Yeh L F; Chen W L; Chen L F; Wang W
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18.
Prenatal diagnosis 2000;20(9):750-3.
2000: Chen C P; Devriendt K; Chern S R; Lee C C; Wang W; Lin S P
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
2000: Chern S R; Chen C P
Molecular prenatal diagnosis of thalassemia in Taiwan.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2000;69(2):103-6.
2000: Chen C P; Chern S R; Wang W
Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies.
Human reproduction (Oxford, England) 2000;15(4):929-34.
1999: Chen C P; Devriendt K; Lee C C; Chen W L; Wang W; Wang T Y
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Prenatal diagnosis 1999;19(10):986-9.
1999: Chen C P; Shih J C; Lee C C; Chen L F; Wang W; Wang T Y
Prenatal diagnosis of a fetus with distal 10q trisomy.
Prenatal diagnosis 1999;19(9):876-8.
1999: Chen C P; Chern S R; Lee C C; Town D D; Chen W L; Wang W
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
Prenatal diagnosis 1999;19(8):783-6.
1999: Chen C P; Chen S R; Wang T Y; Wang W; Hwu Y M
A frame shift mutation in the DNA-binding domain of the androgen receptor gene associated with complete androgen insensitivity, persistent müllerian structures, and germ cell tumors in dysgenetic gonads.
Fertility and sterility 1999;72(1):170-3.
1999: Chen C P; Chern S R; Wang T Y; Wang W; Wang K L; Jeng C J
Androgen receptor gene mutations in 46,XY females with germ cell tumours.
Human reproduction (Oxford, England) 1999;14(3):664-70.
1999: Wang K C; Chen C P; Yang Y C; Wang K G; Hung F Y; Su T H
Stroke complicating pregnancy and the puerperium.
Zhonghua yi xue za zhi = Chinese medical journal; Free China ed 1999;62(1):13-9.
1998: Chen C P; Lee C C; Pan C W; Kir T Y; Chen B F
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis.
Prenatal diagnosis 1998;18(12):1289-93.
1998: Chen C P; Chern S R; Lee C C; Chen W L; Chen M H; Chang K M
De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
Journal of medical genetics 1998;35(12):1050-3.
1998: Chen C P; Wang W; Lin S P; Sheu J C; Tsai J D
Perinatal findings in a male fetus with congenital megacystis and anorectal malformations.
Fetal diagnosis and therapy 1998;13(6):348-51.
1998: Chen C P; Chern S R; Lee C C; Town D D
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence.
Prenatal diagnosis 1998;18(10):1068-74.
1998: Chen C P; Chern S R; Lin S P; Chang P Y; Chang K M; Hsieh F J
Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound.
Prenatal diagnosis 1998;18(9):984-6.
1998: Hwu Y M; Lee R K; Chen C P; Su J T; Chen Y W; Lin S P
Development of hatching blastocysts from immature human oocytes following in-vitro maturation and fertilization using a co-culture system.
Human reproduction (Oxford, England) 1998;13(7):1916-21.
1998: Wang K G; Chen C P; Yang J M; Su T H
Impact of reverse end-diastolic flow velocity in umbilical artery on pregnancy outcome after the 28th gestational week.
Acta obstetricia et gynecologica Scandinavica 1998;77(5):527-31.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y
Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones.
Prenatal diagnosis 1998;18(5):490-5.
1998: Chen C P; Wang T Y; Chuang C Y
Sonographic findings in a fetus with megacystis-microcolon-intestinal hypoperistalsis syndrome.
Journal of clinical ultrasound : JCU 1998;26(4):217-20.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y; Chen M H
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
Prenatal diagnosis 1998;18(4):393-8.
1998: Chen C P; Chern S R; Chuang C Y; Chen B F
Prenatal detection of human cytomegalovirus DNA in fetal ascites by the polymerase chain reaction.
Acta obstetricia et gynecologica Scandinavica 1998;77(4):466-7.
1998: Chen C P; Shih S L; Chuang C Y; Sheu J C; Chen B F
In utero adrenal hemorrhage: clinical and imaging findings.
Acta obstetricia et gynecologica Scandinavica 1998;77(2):239-41.
1998: Chen C P; Hung T H; Jan S W; Jeng C J
Enlarged cisterna magna in the third trimester as a clue to fetal trisomy 18.
Fetal diagnosis and therapy 1998;13(1):29-34.
1998: Chen C P; Chern S R; Shih S L; Chuang C Y; Huang F Y
Kyphomelic dysplasia in two sib fetuses.
Journal of medical genetics 1998;35(1):65-9.
1998: Chen C P; Wang W; Lin S P; Sheu J C; Tzen C Y
Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhage.
American journal of perinatology 1998;15(11):601-5.
1997: Chen C P; Chern S R; Wang T Y; Huang Z D; Huang M C; Chuang C Y
Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia.
Human reproduction (Oxford, England) 1997;12(11):2553-6.
1997: Chen C P; Lee C C; Chen L F; Chuang C Y; Jan S W; Chen B F
Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly.
Journal of medical genetics 1997;34(9):777-8.
1997: Chen C P; Chen S H; Chuang C Y; Lee H C; Hwu Y M; Chang P Y; Chen M L; Chen B F
Clinical and perinatal sonographic features of congenital adrenal cystic neuroblastoma: a case report with review of the literature.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1997;10(1):68-73.
1997: Chen C P; Lin C C; Chuang C Y; Lee C C; Chen W L; Jan S W; Lin S P
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21).
Prenatal diagnosis 1997;17(7):675-80.
1997: Chen C P; Chern S R; Liu F F; Jan S W; Lee C C; Chang Y C; Yue C T
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
Prenatal diagnosis 1997;17(6):571-6.
1997: Chen C P; Shih S L; Liu F F; Jan S W; Jeng C J; Lan C C
Perinatal features of omphalocele-exstrophy-imperforate anus-spinal defects (OEIS complex) associated with large meningomyeloceles and severe limb defects.
American journal of perinatology 1997;14(5):275-9.
1997: Chen C P; Chuang C Y; Chang Y C; Tzen C Y
Type III congenital cystic adenomatoid malformation of the lung detected through maternal serum screening positive for Down's syndrome.
Acta obstetricia et gynecologica Scandinavica 1997;76(4):378-9.
1997: Chen C P; Lee C C; Liu F F; Jan S W; Lin M H; Chen B F
Prenatal diagnosis of cephalothoracopagus janiceps monosymmetros.
Prenatal diagnosis 1997;17(4):384-8.
1997: Chen C P; Shih S L; Liu F F; Jan S W
Cebocephaly, alobar holoprosencephaly, spina bifida, and sirenomelia in a stillbirth.
Journal of medical genetics 1997;34(3):252-5.
1997: Chen C P; Shih S L; Liu F F; Jan S W; Lin Y N; Lan C C
Skeletal deformities of acardius anceps: the gross and imaging features.
Pediatric radiology 1997;27(3):221-5.
1997: Chen C P; Chen H C; Liu F F; Jan S W; Chern S R; Wang T Y; Hung H Y
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascites.
The British journal of dermatology 1997;136(2):267-71.
1997: Chen C P; Liu F F; Jan S W; Wang K G; Lan C C
First report of distal obstructive uropathy and prune-belly syndrome in an infant with amniotic band syndrome.
American journal of perinatology 1997;14(1):31-3.
1997: Chen C P; Chen H C; Liu F F; Jan S W; Lin S P; Sheu J C; Chen B F
Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeus.
The British journal of dermatology 1997;136(1):102-4.
1997: Chen C P; Chern S R; Liu F F; Jan S W; Lee H C; Sheu J C; Lee W T; Wang T Y
Prenatal diagnosis, pathology, and genetic study of fetus in fetu.
Prenatal diagnosis 1997;17(1):13-21.
1997: Chen C; Shih S L; Liu F F; Jan S W; Tsai T C; Chang P Y; Lan C C; Chen C P
In utero urinary bladder perforation, urinary ascites, and bilateral contained urinomas secondary to posterior urethral valves: clinical and imaging findings.
Pediatric radiology 1997;27(1):3-5.
1996: Chen C P; Liu F F; Jan S W; Yang Y C; Lan C C
Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
Prenatal diagnosis 1996;16(12):1137-40.
1996: Chen C P; Liu F F; Jan S W; Lin C L; Lan C C
Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly.
Clinical genetics 1996;50(5):321-6.
1996: Chen C P; Lin S P; Liu F F; Jan S W; Lin S Y; Lan C C
Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome).
American journal of perinatology 1996;13(8):495-8.
1996: Chen C P; Liu F F; Jan S W; Su T H; Lan C C
A concealed penis mimicking penile agenesis in an infant with trisomy 13.
Clinical genetics 1996;50(3):156-8.
1996: Chen C P; Liu F F; Jan S W; Sheu J C; Huang S H; Lan C C
Prenatal diagnosis and perinatal aspects of abdominal wall defects.
American journal of perinatology 1996;13(6):355-61.
1996: Chen C P; Liu F F; Jan S W; Wang K G; Lan C C
Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus.
Prenatal diagnosis 1996;16(7):664-6.
1996: Chen C P; Liu F F; Jan S W; Chen C P; Lan C C
Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.
Journal of medical genetics 1996;33(7):615-7.
1996: Chen C P; Liu F F; Jan S W; Chen C P; Lan C C
Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.
Journal of medical genetics 1996;33(7):615-7.
1996: Kuo Y C; Chen C P; Wang K G
Factors influencing the prolonged second stage and the effects on perinatal and maternal outcomes.
The journal of obstetrics and gynaecology research 1996;22(3):253-7.
1996: Chen C P; Liu F F; Jan S W; Chang P Y; Lin Y N; Lan C C
Ultrasound-guided fluid aspiration and prenatal diagnosis of duplicated hydrometrocolpos with uterus didelphys and septate vagina.
Prenatal diagnosis 1996;16(6):572-6.
1996: Chen C P; Liu F F; Jan S W; Lin S P; Lan C C
CVS-exposed limb deficiency defects with or without other birth defects: presentation of six cases born during a period of nine years.
American journal of medical genetics 1996;63(3):447-53.
1996: Chen C P; Liu F F; Jan S W; Chen C W; Wang K G; Lan C C
Prenatal detection of the separation of the great toe, toe syndactyly, and large bilateral choroid plexus cysts in a fetus with trisomy 18.
American journal of perinatology 1996;13(4):203-5.
1996: Chen C P; Liu F F; Jan S W; Lee C C; Town D D; Lan C C
Cytogenetic evaluation of cystic hygroma associated with hydrops fetalis, oligohydramnios or intrauterine fetal death: the roles of amniocentesis, postmortem chorionic villus sampling and cystic hygroma paracentesis.
Acta obstetricia et gynecologica Scandinavica 1996;75(5):454-8.
1996: Wu R W; Chen C P; Wang K G
Implications of prolonged fetal heart rate deceleration during the second stage of labor.
Journal of the Formosan Medical Association = Taiwan yi zhi 1996;95(3):231-5.
1996: Chen C P; Jan S W; Liu F F; Sheu J C; Huang S H
Echo-guided lymphatic drainage by fine-needle aspiration in persistent isolated septated fetal nuchal cystic hygroma.
Fetal diagnosis and therapy 1996;11(2):150-3.
1996: Chen C P; Liu F F; Jan S W; Lin S P; Lan C C
Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
Prenatal diagnosis 1996;16(3):270-5.
1996: Chen C P; Wang K G
Cryptococcal meningitis in pregnancy.
American journal of perinatology 1996;13(1):35-6.
1996: Chen C P; Chen C W; Wang K G
Spontaneous ovarian hyperstimulation syndrome and hyperprolactinemia in primary hypothyroidism.
Acta obstetricia et gynecologica Scandinavica 1996;75(1):70-1.
1996: Chen C P; Liu F F; Jan S W; Lin Y N; Lan C C
A case of achondrogenesis type IA with an occipital encephalocele.
Genetic counseling (Geneva, Switzerland) 1996;7(3):193-9.
1995: Chen C P; Jan S W; Liu F F; Chiang S; Huang S H; Sheu J C; Wang K G; Lan C C
Prenatal diagnosis of omphalocele associated with umbilical cord cyst.
Acta obstetricia et gynecologica Scandinavica 1995;74(10):832-5.
1995: Chen C P; Wang K G; Su T H; Yang Y C
Acute pancreatitis in pregnancy.
Acta obstetricia et gynecologica Scandinavica 1995;74(8):607-10.
1995: Su T H; Yang J M; Chen C P; Wei H J; Hwu Y M; Yang Y C
Mini-catheter used for bladder drainage following stress-incontinence surgery and the factors relating to drainage failure.
Journal of obstetrics and gynaecology (Tokyo, Japan) 1995;21(4):319-24.
1992: Su T H; Wang Y D; Chen C P; Lei S Y
A conservative surgical treatment of cervical pregnancy with active bleeding--uterine artery ligation and cervicotomy.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 1992;37(4):275-9.
1990: Yu C J; Chen C P; Jeng C J; Yang Y C
Early prenatal diagnosis of Meckel syndrome--a case report.
Zhonghua yi xue za zhi = Chinese medical journal; Free China ed 1990;46(1):53-6.

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