• A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini review
• A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
• A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia
• A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family
• A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias
• A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type
• A single residue of GDF-5 defines binding specificity to BMP receptor IB
• Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families
• Characterization of a novel missense mutation in the prodomain of GDF5, which underlies brachydactyly type C and mild Grebe type chondrodysplasia in a large Pakistani family
• Characterization of an acromesomelic dysplasia, Grebe type case: novel mutation affecting the recognition motif at the processing site of GDF5
• Development and characterization of microsatellite markers for Brazilian four-eyed frogs (genus Pleurodema) endemic to the Caatinga biome
• Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1
• Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan Syndrome
• Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia
• GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations
• Grebe dysplasia - prenatal diagnosis based on rendered 3-D ultrasound images of fetal limbs
• Grebe dysplasia and the spectrum of CDMP1 mutations
• Grebe syndrome
• Grebe syndrome: a rare association with congenital heart disease
• Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5
• Heterogeneity of nonlethal severe short-limbed dwarfism
• Heterozygous manifestations in the heritable disorders of the skeleton
• Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe
• Mechanisms of GDF-5 action during skeletal development
• Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)
• Neonatal Death Dwarfism in a Girl with Distinctive Bone Dysplasia Compatible with Grebe Chondrodysplasia: Analysis by CT Scan-based Phenotype
• Novel homozygous sequence variants in the GDF5 gene underlie acromesomelic dysplasia type-grebe in consanguineous families
• Recurrent mutation in CDMP1 in a family with Grebe chondrodysplasia: broadening the phenotypic manifestation of syndrome in Pakistani population