A molecular and clinical study of Larsen syndrome caused by mutations in FLNB
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S. Robertson | H. Firth | D. Rimoin | C. Kim | J. Fryns | P. Rump | A. Fryer | D. Krakow | L. Bicknell | P. Prontera | D. Cohn | E. Sweeney | Y. Alembik | L. Wilson | Y. Alanay | T. Ravel | J. Pappas | S. Unger | M. Maisenbacher | R. Lachman | Y. Shafeghati | Navid Al-Madani | C. Farrington‐Rock | M. Karimi-Nejad | E. Moran | K. Leask