Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalFertility and Sterility : official journal of the American Fertility Society
Volume95
Issue number8
Pages (from-to)2703-2706
Number of pages4
ISSN0015-0282
DOIs
Publication statusPublished - 2011
MoE publication typeA1 Journal article-refereed

Fields of Science

  • DNA methylation
  • H19
  • MURCS
  • MRKH syndrome
  • Mullerian aplasia
  • SILVER-RUSSELL-SYNDROME
  • MONOZYGOTIC TWINS DISCORDANT
  • KUSTER-HAUSER-SYNDROME
  • CONGENITAL ABSENCE
  • NONCODING RNA
  • MRKH SYNDROME
  • PHENOTYPE
  • HYPOMETHYLATION
  • DEFICIENCY
  • MUTATION
  • 3111 Biomedicine
  • 3123 Gynaecology and paediatrics

Cite this

@article{a0c4b2e88f2f450cb92bdd3ce2b2b713,
title = "Methylation of H19 and its imprinted control region (H19 ICR1) in M{\"u}llerian aplasia",
keywords = "DNA methylation, H19, MURCS, MRKH syndrome, Mullerian aplasia, SILVER-RUSSELL-SYNDROME, MONOZYGOTIC TWINS DISCORDANT, KUSTER-HAUSER-SYNDROME, CONGENITAL ABSENCE, NONCODING RNA, MRKH SYNDROME, PHENOTYPE, HYPOMETHYLATION, DEFICIENCY, MUTATION, 3111 Biomedicine, 3123 Gynaecology and paediatrics",
author = "Maria Sandbacka and Sara Bruce and Mervi Halttunen and Minna Puhakka and Paivi Lahermo and Katariina Hannula-Jouppi and Marita Lipsanen-Nyman and Juha Kere and Kristiina Aittom{\"a}ki and Hannele Laivuori",
year = "2011",
doi = "10.1016/j.fertnstert.2011.03.019",
language = "English",
volume = "95",
pages = "2703--2706",
journal = "Fertility and Sterility : official journal of the American Fertility Society",
issn = "0015-0282",
publisher = "EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC",
number = "8",

}

TY - JOUR

T1 - Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia

AU - Sandbacka, Maria

AU - Bruce, Sara

AU - Halttunen, Mervi

AU - Puhakka, Minna

AU - Lahermo, Paivi

AU - Hannula-Jouppi, Katariina

AU - Lipsanen-Nyman, Marita

AU - Kere, Juha

AU - Aittomäki, Kristiina

AU - Laivuori, Hannele

PY - 2011

Y1 - 2011

KW - DNA methylation

KW - H19

KW - MURCS

KW - MRKH syndrome

KW - Mullerian aplasia

KW - SILVER-RUSSELL-SYNDROME

KW - MONOZYGOTIC TWINS DISCORDANT

KW - KUSTER-HAUSER-SYNDROME

KW - CONGENITAL ABSENCE

KW - NONCODING RNA

KW - MRKH SYNDROME

KW - PHENOTYPE

KW - HYPOMETHYLATION

KW - DEFICIENCY

KW - MUTATION

KW - 3111 Biomedicine

KW - 3123 Gynaecology and paediatrics

U2 - 10.1016/j.fertnstert.2011.03.019

DO - 10.1016/j.fertnstert.2011.03.019

M3 - Article

VL - 95

SP - 2703

EP - 2706

JO - Fertility and Sterility : official journal of the American Fertility Society

JF - Fertility and Sterility : official journal of the American Fertility Society

SN - 0015-0282

IS - 8

ER -