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"陳持平"的相关文件

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机构	日期	题名	作者
亞洲大學	2012-09	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	陳持平;Chen, Chih-Ping
亞洲大學	2012-09	Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation	陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Jun-Wei Su;Yu-Ting Chen;Chen-Chi Lee;Wayseen Wang
亞洲大學	2012-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2	陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Alan Hwa-Ruey Hsieh, ;Hsieh, Alex Hwa-Jiun;Wang, Wayseen
亞洲大學	2012-09	Pure partial monosomy 3p (3p25.3->pter): prenatal diagnosis and array comparative genomic hybridization characterization	陳持平;Chen, Chih-Ping
亞洲大學	2012-09	Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester	陳持平;Chen, Chih-Ping;Wayseen Wang,
亞洲大學	2012-09	Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis	陳持平;Chen, Chih-Ping;Chen-Wen Pan, ;Wang, Wayseen
亞洲大學	2012-09	Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes	陳持平;Chen, Chih-Ping;Dai-Dyi Town, ;Wen-Lin Chen, ;Chen, Li-Feng;Meng-Shan Lee, ;Pan, Chen-Wen;Wang, Wayseen
亞洲大學	2012-09	Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Identification of a deletion mutation in the short flanking repeat region of exon 44 of COL1A1 gene in a fetus with osteogenesis imperfecta type II	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements	陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Chen-Chi Lee, ;Town, Dai-Dyi;Wang, Wayseen
亞洲大學	2012-06	Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Partial monosomy 9p (9p22.2->pter) and partial trisomy 18q (18q21.32->qter) in a female infant with anorectal malformations	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Prenatal findings and the genetic diagnosis of fetal overgrowth disorders:Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Pure distal 9p deletion in a female infant with cerebral palsy	陳持平;Chen, Chih-Ping
亞洲大學	2012-06	Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception	陳持平;Chen,Chih-Ping;Shuan-Pei Lin;Yi-Ning Su;Jian-Pei Huang;Schu-Rern Chern;Jun-Wei Su;Wayseen Wang
亞洲大學	2012-04	Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings	陳持平;Chen, Chih-Ping
亞洲大學	2012-03	Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome	陳持平;Chen, Chih-Ping

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