• <em>FLNB</em> Disorders
• A 100-year-old anatomical specimen presenting with boomerang-like skeletal dysplasia: diagnostic strategies and outcome
• A case of boomerang dysplasia with a novel causative mutation in filamin B: identification of typical imaging findings on ultrasonography and 3D-CT imaging
• Atelosteogenesis I and boomerang dysplasia: a question of nosology
• Atelosteogenesis syndromes: a review, with comments on their pathogenesis
• Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome
• Boomerang bone disease: bilateral dysplasia of ulna and fibula
• Boomerang dysplasia
• Boomerang dysplasia
• Boomerang dysplasia. A new form of neonatal death dwarfism
• Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations
• Comparative analysis of the two extremes of <em>FLNB</em>-mutated autosomal dominant disease spectrum: from clinical phenotypes to cellular and molecular findings
• Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach
• Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity
• Fetal magnetic resonance imaging of skeletal dysplasias
• Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development
• Filamin B mutations cause chondrocyte defects in skeletal development
• Filamin B: The next hotspot in skeletal research?
• Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia
• Giant-cell chondrodysplasia in a male infant with clinical and radiological findings resembling the Piepkorn type of lethal osteochondrodysplasia
• Lethal bone dysplasia in a fetus with manifestations of atelosteogenesis I and Boomerang dysplasia
• Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe "boomerang dysplasia"?
• Mutations in FLNB cause boomerang dysplasia
• Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit
• Prenatal diagnosis of boomerang dysplasia
• Prenatal ultrasonographic description and postnatal pathological findings in atelosteogenesis type 1
• Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNB
• Skeletal dysplasia, boomerang dysplasia
• Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia