A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume21
Issue number9
Pages (from-to)1024-1026
Number of pages3
ISSN1018-4813
DOIs
Publication statusPublished - Sep 2013
MoE publication typeA1 Journal article-refereed

Fields of Science

  • pre-eclampsia
  • linkage
  • maternal phenotype
  • fetal phenotype
  • family study
  • GENOME-WIDE SCAN
  • POPULATION
  • HYPERTENSION
  • COMPONENTS
  • 2P24-P25
  • REVEALS
  • COHORT
  • 3111 Biomedicine

Cite this

@article{222ac447c34a4431b62c140faffc6147,
title = "A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18",
keywords = "pre-eclampsia, linkage, maternal phenotype, fetal phenotype, family study, GENOME-WIDE SCAN, POPULATION, HYPERTENSION, COMPONENTS, 2P24-P25, REVEALS, COHORT, 3111 Biomedicine",
author = "Majander, {Kerttu K.} and Villa, {Pia M.} and Katja Kivinen and Juha Kere and Hannele Laivuori",
year = "2013",
month = "9",
doi = "10.1038/ejhg.2013.6",
language = "English",
volume = "21",
pages = "1024--1026",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "9",

}

TY - JOUR

T1 - A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18

AU - Majander, Kerttu K.

AU - Villa, Pia M.

AU - Kivinen, Katja

AU - Kere, Juha

AU - Laivuori, Hannele

PY - 2013/9

Y1 - 2013/9

KW - pre-eclampsia

KW - linkage

KW - maternal phenotype

KW - fetal phenotype

KW - family study

KW - GENOME-WIDE SCAN

KW - POPULATION

KW - HYPERTENSION

KW - COMPONENTS

KW - 2P24-P25

KW - REVEALS

KW - COHORT

KW - 3111 Biomedicine

U2 - 10.1038/ejhg.2013.6

DO - 10.1038/ejhg.2013.6

M3 - Article

VL - 21

SP - 1024

EP - 1026

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 9

ER -