Showing 1 - 20 results of 58 for search 'Li-Feng Chen', query time: 0.19s Refine Results
  1. 1
    Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses

    Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses by Chih-Ping Chen, Pei-Chen Wu, Fuu-Jen Tsai, Li-Feng Chen, Wayseen Wang

    Published 2012
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line

    45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line by Chih-Ping Chen, Shin-Wen Chen, Chi-Kang Lin, Fang-Tzu Wu, Yun-Yi Chen, Li-Feng Chen, Wayseen Wang

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    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
    Connect to this object online.
    Book
    Save to List
    Saved in:
  4. 4
    Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly

    Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly by Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Yu-Peng Liu, Schu-Rern Chern, Li-Feng Chen, Wayseen Wang

    Published 2011
    Connect to this object online.
    Book
    Save to List
    Saved in:
  5. 5
    Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review

    Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review by Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

    Published 2015
    Connect to this object online.
    Book
    Save to List
    Saved in:
  6. 6
    Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb

    Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis o... by Chih-Ping Chen, Schu-Rern Chern, Chen-Yu Chen, Pei-Chen Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

    Published 2011
    Connect to this object online.
    Book
    Save to List
    Saved in:
  7. 7
    Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome

    Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome by Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Yi-Yung Chen, Pei-Chen Wu, Li-Feng Chen, Wayseen Wang

    Published 2011
    Connect to this object online.
    Book
    Save to List
    Saved in:
  8. 8
    Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome

    Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal... by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  9. 9
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis

    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

    Published 2020
    Connect to this object online.
    Book
    Save to List
    Saved in:
  10. 10
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) result

    Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum scr... by Chih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  11. 11
    Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)

    Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21) by Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

    Published 2013
    Connect to this object online.
    Book
    Save to List
    Saved in:
  12. 12
    Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome

    Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Yu-Ling Kuo, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

    Published 2020
    Connect to this object online.
    Book
    Save to List
    Saved in:
  13. 13
    Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects

    Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

    Published 2019
    Connect to this object online.
    Book
    Save to List
    Saved in:
  14. 14
    High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line

    High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  15. 15
    Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis

    Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q... by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

    Published 2013
    Connect to this object online.
    Book
    Save to List
    Saved in:
  16. 16
    Ventriculomegaly, Intrauterine Growth Restriction, and Congenital Heart Defects as Salient Prenatal Sonographic Findings of Miller-Dieker Lissencephaly Syndrome Associated With Monosomy 17p (17p13.2 → pter) in a Fetus

    Ventriculomegaly, Intrauterine Growth Restriction, and Congenital Heart Defects as Salient Prenatal Sonographic Findings of Miller-Dieker Lissencephaly Syndrome Associated With Mon... by Chih-Ping Chen, Yu-Peng Liu, Shaun-Pei Lin, Ming Chen, Fuu-Jen Tsai, Yu-Ting Chen, Li-Feng Chen, Jonathan Kwei Hwang, Wayseen Wang

    Published 2010
    Connect to this object online.
    Book
    Save to List
    Saved in:
  17. 17
    Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature

    Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature by Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Yu-Ling Kuo, Yen-Ni Chen, Peih-Shan Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

    Published 2015
    Connect to this object online.
    Book
    Save to List
    Saved in:
  18. 18
    Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result

    Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in... by Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

    Published 2021
    Connect to this object online.
    Book
    Save to List
    Saved in:
  19. 19
    Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis

    Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Li-Feng Chen, Wayseen Wang

    Published 2017
    Connect to this object online.
    Book
    Save to List
    Saved in:
  20. 20
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

    Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallo... by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

    Published 2016
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: