53 results on '"Chen, Yi-Yung"'
Search Results
2. Association between maternal benzodiazepine or Z-hypnotic use in early pregnancy and the risk of stillbirth, preterm birth, and small for gestational age: a nationwide, population-based cohort study in Taiwan
3. P‐82: Optimizing Angular Response and Color Estimation for LCD In‐Cell Ambient Light Sensor
4. Mosaic 46,XY,der(15)t(6;15)(q25.1;p12)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and postnatal decrease of the aneuploid cell line with the unbalanced translocation
5. A novel design freeform reflector application applied to natural light illumination system
6. Pupil size detection based on convolution neural network applied on portable pupillometer
7. Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome
8. Detection of a familial 1q21.1 microdeletion and concomitant CHD1Lmutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound
9. Clinical and sonographic risk factors for developing pre-eclampsia refractory to aspirin prophylaxis
10. Low-level mosaic trisomy 21 due to mosaic unbalanced Robertsonian translocation of 46,XX,+21,der(21;21) (q10;q10)/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, cytogenetic discrepancy among various tissues and perinatal progressive decrease of the trisomy 21 cell line
11. Perinatal imaging findings of a fetus with Pfeiffer syndrome and a heterozygous c.1019A>G, p.Tyr340Cys (Y340C) mutation in FGFR2presenting a cloverleaf skull, craniosynostosis and short limbs on prenatal ultrasound mimicking thanatophoric dysplasia type II
12. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
13. Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterinegrowth restriction, intrauterine fetal death, cytogenetic discrepancy betweencultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line
14. Molecular cytogenetic characterization of del(X)(p22.33)mat and de novodup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly
15. Low-level mosaic trisomy 17 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy between cultured and uncultured amniocytes
16. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21and EXT1
17. Rapid Diagnosis of Trisomy 18 Using Uncultured Amniocytes in Late Second Trimester in a Pregnancy with Fetal Congenital Heart Defects, Arthrogryposis, Omphalocele, and Mega Cisterna Magna.
18. Innovative design of light collimator based on a freeform microlens array
19. Heliostat design for the daylighting system
20. VACTERL association with hydrocephalus in a fetus conceived by in vitrofertilization and embryo transfer
21. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
22. Detection of maternal transmission of a splicing mutation in the TSC2gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy
23. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization
24. Modular design optical light pipe with high efficiency
25. Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly
26. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise
27. 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 NEK1gene
28. Characteristics of early-onset neonatal sepsis caused by Escherichia coli
29. Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism
30. Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester
31. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities
32. Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion
33. Using Taguchi method to design LED lamp for zonal lumen density requirement of ENERGY STAR
34. A hemispherical static concentrator with double aspheric compensated lens array for continued collecting sunlight
35. Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIAhaploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction
36. Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome
37. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations
38. Natural light illumination system
39. Acute Fatty Liver of Pregnancy in a Taiwanese Tertiary Care Center: A Retrospective Review
40. The Effects of Absent or Reversed End-diastolic Umbilical Artery Doppler Flow Velocity
41. Spontaneous rupture and massive hemoperitoneum from uterine leiomyomas and adenomyosis in a nongravid and unscarred uterus
42. Prenatal Diagnosis of Limb–Body Wall Complex With Craniofacial Defects.
43. First-trimester sonographic demonstration of digynic triploidy
44. Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novomultiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader–Willi syndrome
45. 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
46. Prenatal Diagnosis and Antenatal History of Total Anomalous Pulmonary Venous Return
47. 179: Decreased placental folate transport in early pregnancy of obese women.
48. Nanoparticles can cross placenta and induce trophoblast apoptosis.
49. Adjustable planar lightguide solar concentrators with liquid-prism structure
50. Secondary optical design for safety light curtains
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