A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability

Maria Rasmussen*, Mette Ramsing, Olav Bjørn Petersen, Ida Vogel, Lone Sunde

*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

10 Citationer (Scopus)

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Keyphrases

Biochemistry, Genetics and Molecular Biology