Showing 1 - 20 results of 24 for search 'Chen-Ju Lin', query time: 0.17s Refine Results
  1. 1
    Impact of Second-Trimester Maternal Serum Screening on Prenatal Diagnosis of Down Syndrome and the use of Amniocentesis in the Taiwanese Population

    Impact of Second-Trimester Maternal Serum Screening on Prenatal Diagnosis of Down Syndrome and the use of Amniocentesis in the Taiwanese Population by Chih-Ping Chen, Chen-Ju Lin, Wayseen Wang

    Published 2005
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  2. 2
    The use of misoprostol in termination of second-trimester pregnancy

    The use of misoprostol in termination of second-trimester pregnancy by Chen-Ju Lin, Shu-Chin Chien, Chih-Ping Chen

    Published 2011
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  3. 3
    Total gestational weight change and rate of change in pregnant Taiwanese women

    Total gestational weight change and rate of change in pregnant Taiwanese women by Fur-Hsing Wen, Ching-Fang Lee, Chen-Ju Lin, Hsien-Ming Lin

    Published 2019
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  4. 4
    Spontaneous Rupture of an Unscarred Uterus Caused by Near-Cornual Pregnancy with Placenta Accreta at 4 Months of Pregnancy

    Spontaneous Rupture of an Unscarred Uterus Caused by Near-Cornual Pregnancy with Placenta Accreta at 4 Months of Pregnancy by Wen-Chu Huang, Fang-Yu Hung, Chih-Ping Chen, Chen-Ju Lin

    Published 2005
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  5. 5
    Ectopic Pregnancy With Oral Contraceptive Use

    Ectopic Pregnancy With Oral Contraceptive Use by Hung-Hung Lin, Ming-Chao Huang, Chen-Ju Lin, Chih-Ping Chen

    Published 2008
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  6. 6
    Huge Primary Vaginal Stone in a Recumbent Woman

    Huge Primary Vaginal Stone in a Recumbent Woman by Chen-Ju Lin, Chih-Ping Chen, Chia-Hsun Wu, Hsin-Yu Chen

    Published 2005
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  7. 7
    Outcome of Pregnancy in Patients with Systemic Lupus Erythematosus

    Outcome of Pregnancy in Patients with Systemic Lupus Erythematosus by Chiong-Hee Wong, Tien-Ling Chen, Chyou-Shen Lee, Chen-Ju Lin, Chih-Ping Chen

    Published 2006
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  8. 8
    Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second-trimester Fetus with Alobar Holoprosencephaly and Trisomy 13

    Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second-trimester Fetus with Alobar Holoprosencephaly and Trisomy 13 by Chih-Ping Chen, Jin-Chung Shih, Chin-Yuan Tzen, Schu-Rern Chern, Chen-Ju Lin, Wayseen Wang

    Published 2008
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  9. 9
    Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association

    Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association by Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Dai-Dyi Town, Wayseen Wang

    Published 2021
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  10. 10
    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
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  11. 11
    The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimester

    The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimester by Tian-Jeau Huang, Chih-Ping Chen, Chen-Ju Lin, Fang-Tzu Wu, Shin-Wen Chen, Shih-Ting Lai, Zhi-Jun Chen

    Published 2023
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  12. 12
    Late-onset fetal bilateral pleural effusions associated with Down syndrome

    Late-onset fetal bilateral pleural effusions associated with Down syndrome by Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Chin Yuan Hsu, Peih-Shan Wu, Chen Chi Lee, Chen Wen Pan, Wayseen Wang

    Published 2018
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  13. 13
    Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3

    Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3 by Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Pei-Chen Wu, Yen-Ni Chen, Chen-Ju Lin, Wen-Ling Chen, Wayseen Wang

    Published 2017
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  14. 14
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia

    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral rad... by Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Fang-Tzu Wu, Schu-Rern Chern, Peih-Shan Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang

    Published 2020
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  15. 15
    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome

    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome by Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

    Published 2017
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  16. 16
    Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency

    Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with s... by Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, Wayseen Wang

    Published 2017
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  17. 17
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication

    Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion a... by Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

    Published 2016
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  18. 18
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review

    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review by Chih-Ping Chen, Ming Chen, Chia-Hsun Wu, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Li-Feng Chen, Wayseen Wang

    Published 2017
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  19. 19
    Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound

    Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

    Published 2018
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  20. 20
    Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome

    Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome by Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Yu-Peng Liu, Yu-Ling Kuo, Yen-Ni Chen, Peih-Shan Wu, Dai-Dyi Town, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

    Published 2014
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