CHARGE Syndrome: New Insights for the Healthcare Professional: 2011 Edition: ScholarlyPaper

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ScholarlyEditions, Jan 9, 2012 - Medical - 18 pages

CHARGE Syndrome: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about CHARGE Syndrome in a compact format.

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From inside the book

 

Selected pages

Contents

Section 1
Section 2
Section 3
Section 4
Section 5
Copyright

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CHARGE Syndrome: New Insights for the Healthcare Professional: 2011 Edition ...

Limited preview - 2012

Common terms and phrases

abnormalities additional information American Journal aplasia aspects of CHD7 atresia cervicocerebral arteriovenous shunt CHARGE syndrome CHD7 functions CHD7 gene CHD7 sites CHD7 Targets CHD8 interacts choanae chromatin immunoprecipitation chromodomain helicase DNA-binding cochlear implantation colleagues published Coloboma cord blood cord blood transplantation Delayed puberty Delayed puberty due Dept DiGeorge sequence including ear anomalies endocrine and molecular gene expression genetic testing Healthcare Professional hearing loss heart defects Histology and synchrotron Human Molecular Genetics hypogonadism hypogonadotrophic hypogonadism hypoparathyroidism hypoplasia indicate that CHD7 Innsbruck interacts with CHD7 Journal of Medical malformations Medical Genetics microtomography missense mutations molecular evaluation molecularly confirmed multipotent multipotent neural crest mutated in CHARGE mutation in CHD7 mutation showing DiGeorge neural crest novo mutation nucleolus patient with CHARGE PBAF to control positive regulator published their study rDNA researchers concluded ribosomal RNA biogenesis showing DiGeorge sequence Successful cord blood temporal bone University of Gottingen Western Reserve University wrote Zentner and colleagues

Bibliographic information

TitleCHARGE Syndrome: New Insights for the Healthcare Professional: 2011 Edition: ScholarlyPaper
ContributorQ. Ashton Acton, PhD
PublisherScholarlyEditions, 2012
ISBN1464915628, 9781464915628
Length18 pages
Subjects › 

Medical / Genetics
  
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