• A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome
• A case report of fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome associated with Klinefelter syndrome and review of the literature
• A case report of Gollop-Wolfgang complex in 12 years old boy
• A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects
• Attenuation of bone morphogenetic protein signaling during amphibian limb development results in the generation of stage-specific defects
• BHLHA9 homozygous duplication in a consanguineous family: A challenge for genetic counseling
• Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada
• Ectrodactyly with fibular aplasia: a separate entity?
• FATCO syndrome--fibular aplasia, tibial campomelia and oligosyndactyly
• Fibular aplasia with ectrodactyly--broadening the clinical spectrum
• Gollop-Wolfgang complex: an alternative to amputation
• Limb salvage treatment for Gollop-Wolfgang complex (femoral bifurcation, complete tibial hemimelia, and hand ectrodactyly)
• Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight
• Three new patients with FATCO: fibular agenesis with ectrodactyly
• Tibial agenesis-ectrodactyly syndrome associated with novel cardiovascular and bronchopulmonary malformations
• Tibial hemimelia and femoral bifurcation