1. Al-Kaissi, A., Ammar, C., Ben Ghachem, M. B., et al. (2003). Facial features and skeletal abnormalities in Larsen syndrome-a study of three generations of a Tunisian family. Swiss Medical Weekly, 133, 625–628.
2. Baasanjav, S., Al-Gazali, L., Hashiguchi, T., et al. (2011). Faulty initiation of proteoglycan synthesis causes cardiac and joint defects. American Journal of Human Genetics, 89, 15–27.
3. Banks, J. T., Wellons, J. C., Tubbs, R. S., et al. (2003). Cervical spine involvement in Larsen’s syndrome: A case illustration. Pediatrics, 111, 199–201.
4. Becker, R., Wegner, R.-D., Kunze, J., et al. (2000). Clinical variability of Larsen syndrome: Diagnosis in a father after sonographic detection of a severely affected fetus. Clinical Genetics, 57, 148–150.
5. Bicknell, L. S., Morgan, T., Bonafe, L., et al. (2005). Mutations in FLNB cause boomerang dysplasia. Journal of Medical Genetics, 42, e43–e46.