| 亞洲大學 |
2012-03 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2012-03 |
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2012-03 |
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular genetic analysis
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2012-03 |
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism
|
陳持平;Chen, Chih-Ping;Yu-Ting Chen, ;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2011-12 |
A 20.5-Mb germline deletion of 13q13.1->q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
|
陳持平;Chen, Chih-Ping;Wang, Wayseen |
| 亞洲大學 |
2011-12 |
Conjoined twins detected in the first trimester: a review
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of left wrist and aplasia of left thumb
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
First trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb-body wall complex
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Management of moderate to severe Alzheimer's disease: Focus on memantine
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Perinatal magnetic resonance imaging demonstration of duplication of the right renal collecting system with ipsilateral hydronephrosis and hydroureter, and contralateral renal hypoplasia
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of mosaic trisomy 9
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Pure interstitial duplication of chromosome 7q (7q31.2->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-12 |
Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
A 24.2-Mb deletion of 4q12->q21.21 characterized by array CGH in a 13�-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
|
陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
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
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
De novo duplication Xq22.1->q24 with a disruption of the NXF geen cluster in a mentally retarded woman with short stature and premature ovarian failure
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses
|
陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of limb-body wall complex with craniofacial defects
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of microvillus inclusion disease
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
Self-injurious behavior associated with trisomy 9p (9p13.1->p24.3)
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-09 |
The use of misoprostol in termination of second-trimester pregnancy
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-08 |
Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis
|
陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wen-Lin Chen, ;Wang, Wayseen |
| 亞洲大學 |
2011-06 |
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Partial monosomy 13q (13q21.32->qter) and partial trisomy 8p (8p12->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p
|
陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Chen-Chi Lee;Wayseen Wang |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-06 |
Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-03 |
Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-03 |
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-03 |
Pathological characterization of a malformed umbilical cord associated with body stalk anomaly
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2011-03 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations
|
陳持平;Chen, Chih-Ping;Yi-Yung Chen, ;Wang, Wayseen |
| 亞洲大學 |
2011-03 |
Unbalanced reciprocal translocations at amniocentesis
|
陳持平;Chen, Chih-Ping;Chen-Wen Pan, |
| 國立臺灣大學 |
2011 |
Mosaic Supernumerary R(1)(P13.2q23.3) in a 10-Year-Old Girl with Epilepsy, Facial Asymmetry, Psychomotor Retardation, Kyphoscoliosis, Dermatofibrosarcoma and Multiple Exostoses
|
陳持平; 林炫沛; 陳明; 蘇怡寧; 陳樹人; 王道遠; 劉育朋; 蔡輔仁; 李貞?; 陳燕彰; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; CHEN, MING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; LIU, YU-PENG; TSAI, FUU-JEN; LEE, CHEN-CHI; CHEN, YANN-JANG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis and Molecular Cytogenetic Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Ring Chromosome 4
|
陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 吳佩臻; 陳麗鳳; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review
|
陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |
