Craniofacial and intraoral phenotype of Robinow syndrome forms - Beiraghi, S; Leon-Salazar, V; Larson, BE; John, MT; Cunningham, ML; Petryk, A; Lohr, JL (Clinical genetics, 2011)
Keywords: Adolescent; Adult; Aged; Alveoli; Biological and medical sciences; Child; craniofacial anomaly; Crowding; Differential diagnosis; Diseases of the osteoarticular system; dwarfism; Dwarfism - genetics; Dwarfism - pathology; Female; Fundamental and applied biological sciences. Psychology; General aspects. Genetic counseling; Genetic disorders; genetics; Genetics of eukaryotes. Biological and molecular evolution; Genotype & phenotype; Heredity; Humans; Limb Deformities, Congenital - genetics; Limb Deformities, Congenital - pathology; Male; Malformations and congenital and or hereditary diseases involving bones. Joint deformations; Maxillofacial Abnormalities - genetics; Maxillofacial Abnormalities - pathology; Medical diagnosis; Medical genetics; Medical sciences; Middle Aged; Molecular and cellular biology; Morphology; Mouth Abnormalities - genetics; Mouth Abnormalities - pathology; Phenotype; Robinow syndrome; Skull - abnormalities; Spine - abnormalities; Spine - pathology; Human; Dwarfism; Oral cavity; Phenotype; Diseases of the osteoarticular system; Genetics; Anomaly; Craniofacial; Robinow syndrome; craniofacial anomaly; Osteochondrodysplasia