Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death

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

Standard

Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death. / Hoeffding, Louise K.; Kock, Kirsten F.; Johnsen, Iben G.; Hansen, Thomas; Werge, Thomas.

In: Case Reports in Perinatal Medicine, 01.2015.

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

Harvard

Hoeffding, LK, Kock, KF, Johnsen, IG, Hansen, T & Werge, T 2015, 'Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death', Case Reports in Perinatal Medicine. https://doi.org/10.1515/crpm-2014-0046

APA

Hoeffding, L. K., Kock, K. F., Johnsen, I. G., Hansen, T., & Werge, T. (2015). Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death. Case Reports in Perinatal Medicine. https://doi.org/10.1515/crpm-2014-0046

Vancouver

Hoeffding LK, Kock KF, Johnsen IG, Hansen T, Werge T. Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death. Case Reports in Perinatal Medicine. 2015 Jan. https://doi.org/10.1515/crpm-2014-0046

Author

Hoeffding, Louise K. ; Kock, Kirsten F. ; Johnsen, Iben G. ; Hansen, Thomas ; Werge, Thomas. / Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death. In: Case Reports in Perinatal Medicine. 2015.

Bibtex

@article{9d70ec2700df45c688b948ddb3032983,
title = "Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death",
author = "Hoeffding, {Louise K.} and Kock, {Kirsten F.} and Johnsen, {Iben G.} and Thomas Hansen and Thomas Werge",
year = "2015",
month = jan,
doi = "10.1515/crpm-2014-0046",
language = "Udefineret/Ukendt",
journal = "Case Reports in Perinatal Medicine",
issn = "2192-8932",
publisher = "De Gruyter Open Ltd.",

}

RIS

TY - JOUR

T1 - Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death

AU - Hoeffding, Louise K.

AU - Kock, Kirsten F.

AU - Johnsen, Iben G.

AU - Hansen, Thomas

AU - Werge, Thomas

PY - 2015/1

Y1 - 2015/1

U2 - 10.1515/crpm-2014-0046

DO - 10.1515/crpm-2014-0046

M3 - Tidsskriftartikel

JO - Case Reports in Perinatal Medicine

JF - Case Reports in Perinatal Medicine

SN - 2192-8932

ER -

ID: 309205334