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Craniosynostoses[electronic resource] :molecular genetics, principles of diagnosis and treatment /

纪录类型:	书目-语言数据,印刷品 : Monograph/item
[NT 15000414] null:	616/.042
[NT 47271] Title/Author:	Craniosynostoses : molecular genetics, principles of diagnosis and treatment // Volume Editors, Maximilian Muenke...[et al.].
[NT 51406] other author:	Muenke, Maximilian.
出版者:	Basel : : Karger,, 2011.
面页册数:	1 online resource (x, 249 p.) : : ill. (some col.)
标题:	Craniosynostoses.
标题:	Craniosynostoses - genetics.
标题:	Craniosynostoses - diagnosis.
标题:	Craniosynostoses - therapy.
ISBN:	9783805595957 (electronic bk.)
ISBN:	3805595956 (electronic bk.)
ISBN:	9783805595940 (hard cover : alk. paper)
ISBN:	3805595948 (hard cover : alk. paper)
ISBN:	9786613153838
ISBN:	6613153834
[NT 15000227] null:	Includes bibliographical references and indexes.
[NT 15000229] null:	Craniosynostosis - the premature fusion of the cranial sutures of an infant's skull - is a challenging and complex condition that can occur as part of a syndrome or in isolation. In the last two decades increased knowledge about the structure and function of the human genome has enabled the discovery of the molecular etiologies of most forms of syndromic craniosynostosis, which in turn has allowed for the analysis of normal and abnormal sutural biology from the atomic to the population-based level. In parallel with the increase in basic biological understanding, advances in clinical diagnosis and treatment have been achieved including improved prenatal imaging technology and craniofacial surgical techniques as well as condition-specific care in specialized hospitals and clinical units. This book represents a comprehensive overview on the subject of craniosynostosis. Its 19 excellent chapters were written by the foremost authorities in the field for a wide range of readers. They cover topics including a historical review, basic biological and molecular studies, the various common and uncommon syndromes, nonsyndromic craniosynostoses, genetic testing, prenatal ultrasonography, and recent methods of neurosurgical and maxillofacial treatment. Both investigators at the bench and clinicians at the operating table will appreciate this timely book which will be the definitive volume on craniosynostosis for many years to come.
电子资源:	http://content.karger.com/produkteDB/produkte.asp?Aktion=ShowEachType&ProduktNr=254775

Craniosynostoses[electronic resource] :molecular genetics, principles of diagnosis and treatment /
Craniosynostosesmolecular genetics, principles of diagnosis and treatment /[electronic resource] :Volume Editors, Maximilian Muenke...[et al.]. - Basel :Karger,2011. - 1 online resource (x, 249 p.) :ill. (some col.) - Monographs in human genetics,vol. 190077-0876 ;. - Monographs in human genetics ;v.17..

Includes bibliographical references and indexes.

Craniosynostosis - the premature fusion of the cranial sutures of an infant's skull - is a challenging and complex condition that can occur as part of a syndrome or in isolation. In the last two decades increased knowledge about the structure and function of the human genome has enabled the discovery of the molecular etiologies of most forms of syndromic craniosynostosis, which in turn has allowed for the analysis of normal and abnormal sutural biology from the atomic to the population-based level. In parallel with the increase in basic biological understanding, advances in clinical diagnosis and treatment have been achieved including improved prenatal imaging technology and craniofacial surgical techniques as well as condition-specific care in specialized hospitals and clinical units. This book represents a comprehensive overview on the subject of craniosynostosis. Its 19 excellent chapters were written by the foremost authorities in the field for a wide range of readers. They cover topics including a historical review, basic biological and molecular studies, the various common and uncommon syndromes, nonsyndromic craniosynostoses, genetic testing, prenatal ultrasonography, and recent methods of neurosurgical and maxillofacial treatment. Both investigators at the bench and clinicians at the operating table will appreciate this timely book which will be the definitive volume on craniosynostosis for many years to come.

ISBN: 9783805595957 (electronic bk.)Subjects--Topical Terms:

488954
Craniosynostoses.

LC Class. No.: RJ482.C73 / C69 2011

Dewey Class. No.: 616/.042

National Library of Medicine Call No.: W1 / MO567P v.19 2011

Craniosynostoses[electronic resource] :molecular genetics, principles of diagnosis and treatment /
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504 $a Includes bibliographical references and indexes.
520 $a Craniosynostosis - the premature fusion of the cranial sutures of an infant's skull - is a challenging and complex condition that can occur as part of a syndrome or in isolation. In the last two decades increased knowledge about the structure and function of the human genome has enabled the discovery of the molecular etiologies of most forms of syndromic craniosynostosis, which in turn has allowed for the analysis of normal and abnormal sutural biology from the atomic to the population-based level. In parallel with the increase in basic biological understanding, advances in clinical diagnosis and treatment have been achieved including improved prenatal imaging technology and craniofacial surgical techniques as well as condition-specific care in specialized hospitals and clinical units. This book represents a comprehensive overview on the subject of craniosynostosis. Its 19 excellent chapters were written by the foremost authorities in the field for a wide range of readers. They cover topics including a historical review, basic biological and molecular studies, the various common and uncommon syndromes, nonsyndromic craniosynostoses, genetic testing, prenatal ultrasonography, and recent methods of neurosurgical and maxillofacial treatment. Both investigators at the bench and clinicians at the operating table will appreciate this timely book which will be the definitive volume on craniosynostosis for many years to come.
588 $a Description based on print version record.
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650 2 2 $a Craniosynostoses $x diagnosis. $3 488956
650 2 2 $a Craniosynostoses $x therapy. $3 488957
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710 2 $a S. Karger (Firm) $3 488806
830 0 $a Monographs in human genetics ; $v v.17. $3 438638
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