Genetisk screening af kommende forældre

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Genetisk screening af kommende forældre. / Smed, Vibe Madsen; Petersen, Olav Bennike Bjørn; Gerdes, Anne-Marie Axø; Diness, Birgitte Rode; Roos, Laura Sønderberg.

In: Ugeskrift for Laeger, Vol. 183, No. 13, V12200933, 29.03.2021.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Smed, VM, Petersen, OBB, Gerdes, A-MA, Diness, BR & Roos, LS 2021, 'Genetisk screening af kommende forældre', Ugeskrift for Laeger, vol. 183, no. 13, V12200933. <https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-03/v12200933_web.pdf>

APA

Smed, V. M., Petersen, O. B. B., Gerdes, A-M. A., Diness, B. R., & Roos, L. S. (2021). Genetisk screening af kommende forældre. Ugeskrift for Laeger, 183(13), [V12200933]. https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-03/v12200933_web.pdf

Vancouver

Smed VM, Petersen OBB, Gerdes A-MA, Diness BR, Roos LS. Genetisk screening af kommende forældre. Ugeskrift for Laeger. 2021 Mar 29;183(13). V12200933.

Author

Smed, Vibe Madsen ; Petersen, Olav Bennike Bjørn ; Gerdes, Anne-Marie Axø ; Diness, Birgitte Rode ; Roos, Laura Sønderberg. / Genetisk screening af kommende forældre. In: Ugeskrift for Laeger. 2021 ; Vol. 183, No. 13.

Bibtex

@article{147d1eee24074033af0605fbcf06e46f,
title = "Genetisk screening af kommende for{\ae}ldre",
abstract = "Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening, ECS). I Denmark, each year estimated 100-180 children are born affected with a serious condition which could have been detected with ECS of the parents. This review describes the considerations and perspectives of a systematic genetic screening programme for prospective parents in the Danish healthcare system.",
keywords = "Child, Genetic Carrier Screening, Genetic Counseling, Genetic Testing, Humans, Parents, Prospective Studies",
author = "Smed, {Vibe Madsen} and Petersen, {Olav Bennike Bj{\o}rn} and Gerdes, {Anne-Marie Ax{\o}} and Diness, {Birgitte Rode} and Roos, {Laura S{\o}nderberg}",
year = "2021",
month = mar,
day = "29",
language = "Dansk",
volume = "183",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "13",

}

RIS

TY - JOUR

T1 - Genetisk screening af kommende forældre

AU - Smed, Vibe Madsen

AU - Petersen, Olav Bennike Bjørn

AU - Gerdes, Anne-Marie Axø

AU - Diness, Birgitte Rode

AU - Roos, Laura Sønderberg

PY - 2021/3/29

Y1 - 2021/3/29

N2 - Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening, ECS). I Denmark, each year estimated 100-180 children are born affected with a serious condition which could have been detected with ECS of the parents. This review describes the considerations and perspectives of a systematic genetic screening programme for prospective parents in the Danish healthcare system.

AB - Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening, ECS). I Denmark, each year estimated 100-180 children are born affected with a serious condition which could have been detected with ECS of the parents. This review describes the considerations and perspectives of a systematic genetic screening programme for prospective parents in the Danish healthcare system.

KW - Child

KW - Genetic Carrier Screening

KW - Genetic Counseling

KW - Genetic Testing

KW - Humans

KW - Parents

KW - Prospective Studies

M3 - Tidsskriftartikel

C2 - 33829993

VL - 183

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 13

M1 - V12200933

ER -

ID: 288283783