Your browser doesn't support javascript.
loading
Imprinting disorders in children born after ART: a Nordic study from the CoNARTaS group.
Henningsen, A A; Gissler, M; Rasmussen, S; Opdahl, S; Wennerholm, U B; Spangsmose, A L; Tiitinen, A; Bergh, C; Romundstad, L B; Laivuori, H; Forman, J L; Pinborg, A; Lidegaard, Ø.
Afiliación
  • Henningsen AA; Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, 2100 Copenhagen, Denmark.
  • Gissler M; Information Services Department, THL Finnish Institute for Health and Welfare, 00270 Helsinki, Finland.
  • Rasmussen S; Department of Neurobiology, Care Sciences and Society, Division of Family Medicine, Karolinska Institute, 17177 Stockholm, Sweden.
  • Opdahl S; Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, 2100 Copenhagen, Denmark.
  • Wennerholm UB; Department of Public Health and Nursing, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
  • Spangsmose AL; Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.
  • Tiitinen A; Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, 2100 Copenhagen, Denmark.
  • Bergh C; Department of Obstetrics and Gynecology, University of Helsinki, Helsinki University Hospital, 00290 Helsinki, Finland.
  • Romundstad LB; Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.
  • Laivuori H; Department of Public Health and Nursing, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
  • Forman JL; Spiren Fertility Clinic, 7491 Trondheim, Norway.
  • Pinborg A; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, 00290 Helsinki, Finland.
  • Lidegaard Ø; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki University Hospital, 00290 Helsinki, Finland.
Hum Reprod ; 35(5): 1178-1184, 2020 05 01.
Article en En | MEDLINE | ID: mdl-32393975
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Síndrome de Silver-Russell Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Síndrome de Silver-Russell Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Año: 2020 Tipo del documento: Article