A flow from screening to diagnostics

Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review

Standard

A flow from screening to diagnostics. / Vogel, Ida; Lou, Stina; Petersen, Olav Bjørn.

Prenatal Genetic Counseling: Practical Support for Prenatal Diagnostics, Decision-Making, and Dealing with Uncertainty. Academic Press, 2022. p. 3-20.

Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review

Harvard

Vogel, I, Lou, S & Petersen, OB 2022, A flow from screening to diagnostics. in Prenatal Genetic Counseling: Practical Support for Prenatal Diagnostics, Decision-Making, and Dealing with Uncertainty. Academic Press, pp. 3-20. https://doi.org/10.1016/B978-0-12-823329-0.00007-6

APA

Vogel, I., Lou, S., & Petersen, O. B. (2022). A flow from screening to diagnostics. In Prenatal Genetic Counseling: Practical Support for Prenatal Diagnostics, Decision-Making, and Dealing with Uncertainty (pp. 3-20). Academic Press. https://doi.org/10.1016/B978-0-12-823329-0.00007-6

Vancouver

Vogel I, Lou S, Petersen OB. A flow from screening to diagnostics. In Prenatal Genetic Counseling: Practical Support for Prenatal Diagnostics, Decision-Making, and Dealing with Uncertainty. Academic Press. 2022. p. 3-20 https://doi.org/10.1016/B978-0-12-823329-0.00007-6

Author

Vogel, Ida ; Lou, Stina ; Petersen, Olav Bjørn. / A flow from screening to diagnostics. Prenatal Genetic Counseling: Practical Support for Prenatal Diagnostics, Decision-Making, and Dealing with Uncertainty. Academic Press, 2022. pp. 3-20

Bibtex

@inbook{e82e28345f034b0db92e37aa27fa0fd1,

title = "A flow from screening to diagnostics",

abstract = "Denmark was one of the first countries in the world to introduce a universal and free-of-charge offer of combined first-trimester screening for chromosomal anomalies to all pregnant women. In the present chapter, we describe the development and current status of the program and reflect on future directions in the era of exome sequencing and cell-based noninvasive testing. Now, prenatal screening programs differ vastly all over the world and even between countries that are often considered comparable, such as Denmark and Norway. In this chapter, we will present a few such comparisons but will focus mainly on a thorough description of the Danish context. The aim is to give the reader a point of reference to consider and compare their specific, national context.",

keywords = "cFTS, combined screening, Danish context, Exome sequencing, NIPT, pregnant women",

author = "Ida Vogel and Stina Lou and Petersen, {Olav Bj{\o}rn}",

year = "2022",

doi = "10.1016/B978-0-12-823329-0.00007-6",

language = "English",

isbn = "9780128233313",

pages = "3--20",

booktitle = "Prenatal Genetic Counseling",

publisher = "Academic Press",

address = "United States",

}

RIS

TY - CHAP

T1 - A flow from screening to diagnostics

AU - Vogel, Ida

AU - Lou, Stina

AU - Petersen, Olav Bjørn

PY - 2022

Y1 - 2022

N2 - Denmark was one of the first countries in the world to introduce a universal and free-of-charge offer of combined first-trimester screening for chromosomal anomalies to all pregnant women. In the present chapter, we describe the development and current status of the program and reflect on future directions in the era of exome sequencing and cell-based noninvasive testing. Now, prenatal screening programs differ vastly all over the world and even between countries that are often considered comparable, such as Denmark and Norway. In this chapter, we will present a few such comparisons but will focus mainly on a thorough description of the Danish context. The aim is to give the reader a point of reference to consider and compare their specific, national context.

AB - Denmark was one of the first countries in the world to introduce a universal and free-of-charge offer of combined first-trimester screening for chromosomal anomalies to all pregnant women. In the present chapter, we describe the development and current status of the program and reflect on future directions in the era of exome sequencing and cell-based noninvasive testing. Now, prenatal screening programs differ vastly all over the world and even between countries that are often considered comparable, such as Denmark and Norway. In this chapter, we will present a few such comparisons but will focus mainly on a thorough description of the Danish context. The aim is to give the reader a point of reference to consider and compare their specific, national context.

KW - cFTS

KW - combined screening

KW - Danish context

KW - Exome sequencing

KW - NIPT

KW - pregnant women

U2 - 10.1016/B978-0-12-823329-0.00007-6

DO - 10.1016/B978-0-12-823329-0.00007-6

M3 - Book chapter

AN - SCOPUS:85139298562

SN - 9780128233313

SP - 3

EP - 20

BT - Prenatal Genetic Counseling

PB - Academic Press

ER -

ID: 327139664

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