Hasil Pencarian - Jun‐Wei Su

Perbaiki Hasil
  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... oleh Chih-Ping Chen, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2011-12-01
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  2. 2
    Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios

    Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios oleh Chih-Ping Chen, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2013-12-01
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  3. 3
    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. oleh Xiao-Bo Yu, Jun-Wei Su, Xiu-Yang Li, Gao Chen

    Diterbitkan 2014-01-01
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  4. 4
    Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth

    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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  5. 5
    First-trimester prenatal diagnosis of Ellis–van Creveld syndrome

    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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  6. 6
    Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review

    Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review oleh Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2013-12-01
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  7. 7
    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 oleh Chih-Ping Chen, Tsung-Hsien Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang

    Diterbitkan 2012-12-01
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  8. 8
    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 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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  9. 9
    Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF–ET

    Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF–ET oleh Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2013-06-01
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  10. 10
    Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

    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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  11. 11
    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... 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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  12. 12
    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 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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  13. 13
    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 oleh Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2012-06-01
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  14. 14
    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 single colony

    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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  15. 15
    Mosaic isochromosome 20q detected at amniocentesis: A likely cell culture artifact

    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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  16. 16
    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 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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  17. 17
    VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer

    VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer oleh Chih-Ping Chen, Tung-Yao Chang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Diterbitkan 2013-12-01
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  18. 18
    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 oleh Chiung-Yi Yeh, Jun-Wei Su, Cherry Yin-Yi Chang, Chih-Yi Yang, Wu-Chou Lin, Chien-Chu Huang

    Diterbitkan 2022-11-01
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  19. 19
    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 oleh Chih-Ping Chen, Yi-Ning Su, Chen-Yu Chen, Jun-Wei Su, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang

    Diterbitkan 2012-09-01
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  20. 20
    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... 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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