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

8 Citations (Scopus)

Fingerprint

Dive into the research topics of 'A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability'. Together they form a unique fingerprint.

Keyphrases

Biochemistry, Genetics and Molecular Biology