[PDF.46hz] Craniosynostoses: Molecular Genetics, Principles of Diagnosis, and Treatment (Monographs in Human Genetics, Vol. 19)

Craniosynostoses: Molecular Genetics, Principles of Diagnosis, and Treatment (Monographs in Human Genetics, Vol. 19)

[PDF.an90] Craniosynostoses: Molecular Genetics, Principles of Diagnosis, and Treatment (Monographs in Human Genetics, Vol. 19)

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 | #8074747 in Books |  2011-03-07 | Original language:English |  10.00 x7.50 x.75l, | File type: PDF | 250 pages

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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 ato...

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