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Describes the use of combined biochemical markers to screen for neural tube and chromosomal defects, presents the latest developments relating to testing fetal cells in the mother's blood, and reviews major advances in molecular genetics that permit prenatal carrier detection and presymptomatic and predictive testing. Much has changed since the publication of the fourth edition. The new technologies of fetal MRI, 3-D ultrasound, and real time PCR of fetal DNA in maternal circulation yield crucial information, while integrated screening of data from the first and second trimesters coupled with ultrasound now produces a 94 percent detection rate.
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Previews available in: English
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Genetic disorders and the fetus: diagnosis, prevention, and treatment
2004, Johns Hopkins University Press
in English
- 5th ed.
0801879280 9780801879289
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Includes bibliographical references and index.
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- Created October 17, 2008
- 9 revisions
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| January 16, 2025 | Edited by MARC Bot | import existing book |
| August 11, 2024 | Edited by MARC Bot | import existing book |
| December 7, 2020 | Edited by MARC Bot | import existing book |
| October 8, 2020 | Edited by ImportBot | import existing book |
| October 17, 2008 | Created by ImportBot | Imported from bcl_marc record |

