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Book Chapter: Genetics

TitleGenetics
Authors
Issue Date2010
Citation
The Growing Spine: Management of Spinal Disorders in Young Children, 2010, p. 49-59 How to Cite?
AbstractDNA is The blueprint of our human body. Variations in DNA are The source for The phe-notypes of different individuals. The two most common types of variations, also called polymorphisms, are microsatellites and single nucleotide polymorphisms (SNPs) in our DNA. Mendelian disease refers to a simple form of disease in which alternation or mutation in a single gene is enough for its manifestation. Linkage analysis has been proven to be a use-ful method for studying this type of disease. Complex genetic disorders are caused by multiple genes with small effects combined with environmental factors. Candidate gene and genome-wide association studies using case-control design are best used to analyze these disorders. Idiopathic scoliosis is likely a complex genetic disorder. With The recent new developments in human genetics The cause of idiopathic and con-genital scoliosis will most likely be elucidated in The not-too-distant future. © Springer-Verlag Berlin Heidelberg 2011.
Persistent Identifierhttp://hdl.handle.net/10722/244159

 

DC FieldValueLanguage
dc.contributor.authorCheung, Kenneth M C-
dc.contributor.authorHo, Daniel W H-
dc.contributor.authorSong, You Qiang-
dc.date.accessioned2017-08-31T08:56:13Z-
dc.date.available2017-08-31T08:56:13Z-
dc.date.issued2010-
dc.identifier.citationThe Growing Spine: Management of Spinal Disorders in Young Children, 2010, p. 49-59-
dc.identifier.urihttp://hdl.handle.net/10722/244159-
dc.description.abstractDNA is The blueprint of our human body. Variations in DNA are The source for The phe-notypes of different individuals. The two most common types of variations, also called polymorphisms, are microsatellites and single nucleotide polymorphisms (SNPs) in our DNA. Mendelian disease refers to a simple form of disease in which alternation or mutation in a single gene is enough for its manifestation. Linkage analysis has been proven to be a use-ful method for studying this type of disease. Complex genetic disorders are caused by multiple genes with small effects combined with environmental factors. Candidate gene and genome-wide association studies using case-control design are best used to analyze these disorders. Idiopathic scoliosis is likely a complex genetic disorder. With The recent new developments in human genetics The cause of idiopathic and con-genital scoliosis will most likely be elucidated in The not-too-distant future. © Springer-Verlag Berlin Heidelberg 2011.-
dc.languageeng-
dc.relation.ispartofThe Growing Spine: Management of Spinal Disorders in Young Children-
dc.titleGenetics-
dc.typeBook_Chapter-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/978-3-540-85207-0_4-
dc.identifier.scopuseid_2-s2.0-84892035982-
dc.identifier.spage49-
dc.identifier.epage59-

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