Showing 1 - 20 results of 34 for search 'Liang-Kai Wang', query time: 0.20s Refine Results
  1. 1
    Dual-Camera Based Video Morphing and its Application on Video Conference
    by Liang-Kai Wang, 王亮凱
    Published 2006
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  2. 2
    Application of data mining and statistic techniques in customer satisfaction
    by Liang-Kai Wang, 王亮凱
    Published 2008
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  3. 3
    Effect of Sesame Oil against Thioacetamide-induced Hepatic Injury in Rats
    by Liang-Kai Wang, 王亮凱
    Published 2009
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  4. 4
    Spontaneous rupture and massive hemoperitoneum from uterine leiomyomas and adenomyosis in a nongravid and unscarred uterus
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  5. 5
    The reliability of transabdominal cervical length measurement in a low-risk obstetric population: Comparison with transvaginal measurement
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  6. 6
    Design of High-Security USB Flash Drives Based on Chaos Authentication
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  7. 7
    Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization
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  8. 8
    First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
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    Article
  9. 9
    Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion
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  10. 10
    Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1
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  11. 11
    Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly
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  12. 12
    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
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  13. 13
    Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion
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  14. 14
    Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy
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  15. 15
    Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister–Killian syndrome detected by amniocentesis
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  16. 16
    Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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  17. 17
    Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization
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  18. 18
    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
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  19. 19
    22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound
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  20. 20
    Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review
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