• A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature
• 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 new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation
• A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3
• A pair of sibs with tibial hemimelia born to phenotypically normal parents
• A rare case of limb deficiency syndrome: Gollop WolfGang syndrome
• Agenesis of tibia with ectrodactyly/Gollop-Wolfgang complex associated with congenital heart malformations and additional skeletal abnormalities
• Aplasia of the tibia with bifurcation of the femur and ectrodactyly: evidence for an autosomal recessive type
• Aplasia of tibia with split-hand/split-foot deformity. Report of six families with 35 cases and considerations about variability and penetrance
• 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
• Bifurcation of the femur with tibial agenesis and additional anomalies
• Bilateral congenital split hand with tibial aplasia
• Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritance
• Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada
• Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984)
• Distal trisomy 10q and limb defects
• Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
• Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
• Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis
• Familial ectrodactyly syndrome in a nigerian child: a case report
• Familial occurrence of bifid femur and monodactylous ectrodactyly
• FATCO syndrome--fibular aplasia, tibial campomelia and oligosyndactyly
• Fatty filum terminale and low-lying conus medullaris in Gollop-Wolfgang complex: a case report and review of literature
• Femoral bifurcation and bilateral tibial hemimelia: case report
• Fibular aplasia with ectrodactyly
• Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion
• Gollop-Wolfgang complex and cloacal exstrophy, a strange association
• Gollop-Wolfgang Complex in a baby born to an epileptic mother treated with valproic acid during pregnancy
• Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in <em>WNT11</em>
• Gollop-Wolfgang complex: an alternative to amputation
• Gollop-Wolfgang Complex: Clinical and Imaging Implications
• Gollop-Wolfgang syndrome
• Hypohidrotic ectodermal dysplasia with tibial aplasia
• Infant with midline thoracoabdominal schisis and limb defects
• Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex
• Limb salvage treatment for Gollop-Wolfgang complex (femoral bifurcation, complete tibial hemimelia, and hand ectrodactyly)
• Lower Extremity Surgical Treatment to Improve Function in a Patient with Gollop-Wolfgang Complex: A Case Report
• Monodactylous splithand-splitfoot. A malformation occurring in three distinct genetic types
• Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight
• Prenatal diagnosis of Gollop-Wolfgang complex
• SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably
• Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature
• Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families
• Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: two cases and expansion of the phenotype to radial agenesis
• Tetra-oligodactyly with bilateral aplasia and hypoplasia of long bones of upper and lower limbs: a variable manifestation of the syndrome of ectrodactyly with tibial aplasia
• The anatomy of a congenitally short limb with clubfoot and ectrodactyly
• The effects of 5-fluorouracil and 5-fluorodeoxyuridine used alone and in combination with normal nucleic acid precursors on development of mice in lines selected for low and high expression of Strong's luxoid gene
• The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency
• Three new patients with FATCO: fibular agenesis with ectrodactyly
• Tibial agenesis-ectrodactyly syndrome associated with novel cardiovascular and bronchopulmonary malformations
• Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian family
• Tibial aplasia-hypoplasia and ectrodactyly in monozygotic twins with a discordant phenotype
• Tibial developmental field defect in valproic acid embryopathy: Report on three cases
• Tibial hemimelia and femoral bifurcation
• Tibial hypoplasia with a bifid tibia: an unclassified tibial hemimelia
• Unilateral cleft hand (lobster-claw deformity)