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机构 日期 题名 作者
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

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