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Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
- Brian P. Kelley
- , Fransiska Malfait
- , Luisa Bonafe
- , Dustin Baldridge
- , Erica Homan
- , Sofie Symoens
- , Andy Willaert
- , Nursel Elcioglu
- , Lionel Van Maldergem
- , Christine Verellen-Dumoulin
- , Yves Gillerot
- , Dobrawa Napierala
- , Deborah Krakow
- , Peter Beighton
- , Andrea Superti-Furga
- , Anne De Paepe
- , Brendan Lee
- Institute of Clinical and Translational Sciences (ICTS)
- Division of Genetics and Genomic Medicine
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- DBBS - Biomedical Informatics and Data Science
- DBBS - Molecular Genetics and Genomics
- Intellectual and Developmental Disabilities Research Center (IDDRC)
- Edison Family Center for Genome Sciences & Systems Biology
Research output: Contribution to journal › Article › peer-review
166
Scopus
citations