Showing 1 - 20 results of 50 for search 'Jun-Wei Su', query time: 0.06s Refine Results
  1. 1
    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

    First-trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb–body w... by Chih-Ping Chen, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang

    Published 2011-12-01
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  2. 2
    Short-term effects of particulate matter on stroke attack: meta-regression and meta-analyses.

    Short-term effects of particulate matter on stroke attack: meta-regression and meta-analyses. by Xiao-Bo Yu, Jun-Wei Su, Xiu-Yang Li, Gao Chen

    Published 2014-01-01
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  3. 3
    Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth

    Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth by Chih-Ping Chen, Shuenn-Dyh Chang, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang

    Published 2013-09-01
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  4. 4
    First-trimester prenatal diagnosis of Ellis–van Creveld syndrome

    First-trimester prenatal diagnosis of Ellis–van Creveld syndrome by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2012-12-01
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  5. 5
    Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother

    Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother by Chih-Ping Chen, Tsung-Hsien Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang

    Published 2012-12-01
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  6. 6
    Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism

    Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013-03-01
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  7. 7
    Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

    Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis by Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013-12-01
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  8. 8
    Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II

    Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straigh... by Chih-Ping Chen, Tung-Yao Chang, Ming-Huei Lin, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013-09-01
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  9. 9
    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

    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 by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013-03-01
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  10. 10
    Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II

    Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2012-06-01
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  11. 11
    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

    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 by Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2012-06-01
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  12. 12
    Cervical pregnancy: a case report of hysteroscopic resection and balloon compression combined with systematic methotrexate treatment

    Cervical pregnancy: a case report of hysteroscopic resection and balloon compression combined with systematic methotrexate treatment by Chiung-Yi Yeh, Jun-Wei Su, Cherry Yin-Yi Chang, Chih-Yi Yang, Wu-Chou Lin, Chien-Chu Huang

    Published 2022-11-01
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  13. 13
    Pure partial monosomy 3p (3p25.3 → pter): Prenatal diagnosis and array comparative genomic hybridization characterization

    Pure partial monosomy 3p (3p25.3 → pter): Prenatal diagnosis and array comparative genomic hybridization characterization by Chih-Ping Chen, Yi-Ning Su, Chen-Yu Chen, Jun-Wei Su, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang

    Published 2012-09-01
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  14. 14
    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

    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... by Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang

    Published 2012-06-01
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  15. 15
    Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction

    Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction by Chih-Ping Chen, Chin-Yuan Hsu, Yi-Ning Su, Tao-Yeuan Wang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013-03-01
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  16. 16
    Prenatal diagnosis of trisomy 8 mosaicism

    Prenatal diagnosis of trisomy 8 mosaicism by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang

    Published 2012-12-01
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  17. 17
    Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis

    Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis by Chih-Ping Chen, Yi-Ning Su, Jun-Wei Su, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang

    Published 2013-03-01
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  18. 18
    Osteogenesis imperfecta type IV: Prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome

    Osteogenesis imperfecta type IV: Prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Ming-Huei Lin, Jun-Wei Su, Wayseen Wang

    Published 2012-06-01
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  19. 19
    Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta

    Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta by Chih-Ping Chen, Chen-Ju Lin, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang

    Published 2013-06-01
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  20. 20
    Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization

    Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridizatio... by Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang

    Published 2013-06-01
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