Molecular genetics of pediatric orthopaedic disorders. ([2015])

• Record Type: Book
• Further Information: Note: Carol A. Wise, Jonathan J. Rios, editors.
• Editors: Wise, Carol A; Rios, Jonathan J
• Contents: Overview of next generation, high-throughput molecular genetic methods -- Neurofibromin in skeletal development -- Molecular genetics of congenital multiple large joint dislocation -- DMP-1 in postnatal bone development -- The genetic architecture of idiopathic scoliosis -- Insights into the genetics of clubfoot -- Classification and etiologic dissection of vertebral segmentation anomalies -- Genetic and environmental interaction in malformation of the vertebral column -- Somatic mutations in overgrowth syndromes -- Index.
• Publisher Details: New York : Springer
• Publication Date: 2015
• Extent: 1 online resource, illustrations
• Subjects: 618.927; Medicine; Pediatric orthopedics; Human molecular genetics; MEDICAL -- Gynecology & Obstetrics; Human molecular genetics; Pediatric orthopedics; Muscular Diseases -- genetics; Bone Diseases -- genetics; Child; Biomedicine; Human Genetics; Orthopedics; Biomedicine general; Medical -- Orthopedics; Medical -- General; Orthopaedics & fractures; Medical research; Human genetics; Orthopedics; Medical -- Genetics; Medical genetics; Electronic books
• Languages: English
• ISBNs: 9781493921690
• Related ISBNs: 149392169X; 9781493921683; 1493921681; 9781493921683
• Notes: Note: ReferencesChapter-3; Molecular Genetics of Congenital Multiple Large Joint Dislocation; Definition of Large Joint Dislocation; Mendelian Disorders of Congenital Large Joint Dislocation; Autosomal Dominant Disorders; Larsen syndrome (OMIM 150250) ; The Ehlers Danlos Syndrome (EDS) Arthrochalasia Type; Spondyloepimetaphyseal Dysplasia with Joint Laxity-2; Autosomal Recessive Disorders; Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1; Autosomal Recessive Multiple Joint Dislocations-CHST3 Type; Multiple Joint Dislocations-B3GAT3 Type; Desbuquois Dysplasia.; Note: Vendor-supplied metadata.
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