1. Larsen LJ, Schottstaedt ER, Bost FC. Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr. 1950;37(4):574–81.
2. Bonaventure J, Lasselin C, Mellier J, Cohen-Solal L, Maroteaux P. Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome. J Med Genet. 1992;29(7):465–70.
3. Zhang D, Herring JA, Swaney SS, McClendon TB, Gao X, Browne RH, et al. Mutations responsible for Larsen syndrome cluster in the FLNB protein. J Med Genet. 2006;43(5):e24.
4. Vujic M, Hallstensson K, Wahlstrom J, Lundberg A, Langmaack C, Martinson T. Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus. Am J Hum Genet. 1995;57(5):1104–13.
5. Benjamin AA, Goldberg MJ. Chapter 8: Syndromes of orthopaedic importance. In: Stuart Weinstein JF, editor. Lovell and winter’s pediatric orthopaedics. 7th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2014.