Larsen Syndrome and the Hip
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-12003-0_26
Reference81 articles.
1. Harris R, Cullen CH. Autosomal dominant inheritance in Larsen’s syndrome. Clin Genet. 1971;2:87–90.
2. Larsen LJ, Schottstaedt ER, Bost FC. Multiple congenital dislocations associated with characteristic facial abnormality. J Pediatr. 1950;37:574–81.
3. Bicknell LS, Farrington-Rock C, Shafeghati Y, Rump P, Alanay Y, Alembik Y, Al-Madani N, Firth H, Karimi-Nejad MH, Kim CA, Leask K, Maisenbacher M, Moran E, Pappas JG, Prontera P, Ravel T, Fryns JP, Sweeney E, Fryer A, Unger S, Wilson LC, Lachman RS, Rimoin DL, Cohn DH, Krackow D, Robertson SP. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB. J Med Genet. 2007;44:89–98.
4. Robertson S. FLNB-related disorders. Gene Reviews. 2013. https://www.ncbi.nlm.nih.gov/books/NBK2534/ . Accessed 2 Mar 2018.
5. Trigueros AP, Vazquez JLV, de Miguel GFD. Larsen’s syndrome: report of three cases in the one family, mother and two offspring. Acta Orthop Scand. 1978;49:582–8.
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