| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1028-4559(09)60188-1 |
| P698 | PubMed publication ID | 17272206 |
| P2093 | author name string | Esther Shih-Chu Ho | |
| Min-Hui Chen | |||
| Min-Min Chou | |||
| Jenn-Jhy Tseng | |||
| Feng-Chu Lo | |||
| Hui-Yu Lai | |||
| P2860 | cites work | The use of a rapid in situ technique for third-trimester diagnosis of trisomy 18. | Q43422576 |
| Changes in the utilization of prenatal diagnosis | Q44119649 | ||
| P433 | issue | 1 | |
| P921 | main subject | genetic amniocentesis | Q122890592 |
| amniocentesis | Q473768 | ||
| P304 | page(s) | 39-41 | |
| P577 | publication date | 2006-03-01 | |
| P1433 | published in | Taiwanese Journal of Obstetrics & Gynecology | Q26853808 |
| P1476 | title | Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004. | |
| P478 | volume | 45 |
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| Q37233919 | The importance of rapid aneuploidy screening and prenatal diagnosis in the detection of numerical chromosomal abnormalities |
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| Q51803633 | Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. |
| Q55427016 | Why do patients decline amniocentesis? Analysis of factors influencing the decision to refuse invasive prenatal testing. |
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