Hasil Pencarian - Chih-Ping Chen

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  1. 1
    Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcome

    Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcome oleh Chih-Ping Chen

    Diterbitkan 2021-09-01
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  2. 2
    Placental Abnormalities and Preeclampsia in Trisomy 13 Pregnancies

    Placental Abnormalities and Preeclampsia in Trisomy 13 Pregnancies oleh Chih-Ping Chen

    Diterbitkan 2009-03-01
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  3. 3
    Recurrent neural tube defect and craniorachischisis detected in the first trimester and associated with maternal smoking

    Recurrent neural tube defect and craniorachischisis detected in the first trimester and associated with maternal smoking oleh Chih-Ping Chen

    Diterbitkan 2024-03-01
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  4. 4
    Chromosomal Abnormalities Associated with Neural Tube Defects (I): Full Aneuploidy

    Chromosomal Abnormalities Associated with Neural Tube Defects (I): Full Aneuploidy oleh Chih-Ping Chen

    Diterbitkan 2007-12-01
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  5. 5
    Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birth

    Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome... oleh Chih-Ping Chen

    Diterbitkan 2024-01-01
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  6. 6
    False positive non-invasive prenatal testing (NIPT) for partial deletion of chromosome 7q in a pregnancy associated with maternal uterine fibroids and a normal maternal blood cytogenetic result

    False positive non-invasive prenatal testing (NIPT) for partial deletion of chromosome 7q in a pregnancy associated with maternal uterine fibroids and a normal maternal blood cytog... oleh Chih-Ping Chen

    Diterbitkan 2024-03-01
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  7. 7
    Craniorachischisis in a stillbirth associated with maternal smoking

    Craniorachischisis in a stillbirth associated with maternal smoking oleh Chih-Ping Chen

    Diterbitkan 2024-01-01
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  8. 8
    Prenatal Diagnosis and Genetic Counseling for Mosaic Trisomy 13

    Prenatal Diagnosis and Genetic Counseling for Mosaic Trisomy 13 oleh Chih-Ping Chen

    Diterbitkan 2010-03-01
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  9. 9
    Chromosomal abnormalities associated with fetal megacystis

    Chromosomal abnormalities associated with fetal megacystis oleh Chih-Ping Chen

    Diterbitkan 2024-01-01
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  10. 10
    False positive non-invasive prenatal testing (NIPT) for trisomy 21 in vanishing twin syndrome pregnancy: A comparison of the NIPT results performed in different gestations

    False positive non-invasive prenatal testing (NIPT) for trisomy 21 in vanishing twin syndrome pregnancy: A comparison of the NIPT results performed in different gestations oleh Chih-Ping Chen

    Diterbitkan 2023-11-01
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  11. 11
    Low-level mosaic trisomy 17 at amniocentesis can be associated with a favorable pediatric outcome: The follow-ups of three consecutive cases

    Low-level mosaic trisomy 17 at amniocentesis can be associated with a favorable pediatric outcome: The follow-ups of three consecutive cases oleh Chih-Ping Chen

    Diterbitkan 2021-07-01
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  12. 12
    Chromosomal Abnormalities Associated With Omphalocele

    Chromosomal Abnormalities Associated With Omphalocele oleh Chih-Ping Chen

    Diterbitkan 2007-03-01
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  13. 13
    Molecular cytogenetic analysis of mosaic 45,X/46,X,r(X) at amniocentesis in a fetus with hydrops fetalis

    Molecular cytogenetic analysis of mosaic 45,X/46,X,r(X) at amniocentesis in a fetus with hydrops fetalis oleh Chih-Ping Chen

    Diterbitkan 2024-09-01
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  14. 14
    Syndromes, Disorders and Maternal Risk Factors Associated With Neural Tube Defects (VI)

    Syndromes, Disorders and Maternal Risk Factors Associated With Neural Tube Defects (VI) oleh Chih-Ping Chen

    Diterbitkan 2008-09-01
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  15. 15
    Genetic testing using fetal urine at vesicocentesis in case of fetal megacystis

    Genetic testing using fetal urine at vesicocentesis in case of fetal megacystis oleh Chih-Ping Chen

    Diterbitkan 2024-03-01
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  16. 16
    Genetic counseling of mosaicism for a duplication due to partial trisomy in a cell line with 46 chromosomes associated with a normal cell line at amniocentesis

    Genetic counseling of mosaicism for a duplication due to partial trisomy in a cell line with 46 chromosomes associated with a normal cell line at amniocentesis oleh Chih-Ping Chen

    Diterbitkan 2024-09-01
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  17. 17
    Prenatal Diagnosis, Fetal Surgery, Recurrence Risk and Differential Diagnosis of Neural Tube Defects

    Prenatal Diagnosis, Fetal Surgery, Recurrence Risk and Differential Diagnosis of Neural Tube Defects oleh Chih-Ping Chen

    Diterbitkan 2008-09-01
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  18. 18
    Syndromes, Disorders and Maternal Risk Factors Associated With Neural Tube Defects (VII)

    Syndromes, Disorders and Maternal Risk Factors Associated With Neural Tube Defects (VII) oleh Chih-Ping Chen

    Diterbitkan 2008-09-01
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  19. 19
    Genetic counseling of mosaicism for a deletion due to partial monosomy in a cell line with 46 chromosomes associated with a normal cell line at amniocentesis

    Genetic counseling of mosaicism for a deletion due to partial monosomy in a cell line with 46 chromosomes associated with a normal cell line at amniocentesis oleh Chih-Ping Chen

    Diterbitkan 2024-09-01
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  20. 20
    Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly

    Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly oleh Chih-Ping Chen

    Diterbitkan 2024-01-01
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