Hasil Pencarian - Jun‐Wei Su
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Short-term effects of particulate matter on stroke attack: meta-regression and meta-analyses. oleh Xiao-Bo Yu, Jun-Wei Su, Xiu-Yang Li, Gao Chen
Diterbitkan 2014-01-01
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Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth oleh Chih-Ping Chen, Shuenn-Dyh Chang, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang
Diterbitkan 2013-09-01
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First-trimester prenatal diagnosis of Ellis–van Creveld syndrome oleh Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Diterbitkan 2012-12-01
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Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis oleh Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Diterbitkan 2013-12-01
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Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straigh... oleh Chih-Ping Chen, Tung-Yao Chang, Ming-Huei Lin, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Diterbitkan 2013-09-01
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Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome oleh Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Diterbitkan 2013-03-01
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Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a sin... oleh Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang
Diterbitkan 2013-06-01
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Mosaic isochromosome 20q detected at amniocentesis: A likely cell culture artifact oleh Chih-Ping Chen, Shuenn-Dyh Chang, Yu-Ting Chen, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang
Diterbitkan 2012-12-01
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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 oleh Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Diterbitkan 2012-06-01
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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 i... oleh Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang
Diterbitkan 2012-06-01
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