كتاب
Congenital heart disease: molecular diagnostics
العنوان: | Congenital heart disease: molecular diagnostics |
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المساهمون: | Kearns-Jonker, Mary. |
بيانات النشر: | Totowa, N.J. : Humana Press, c2006. |
سنة النشر: | 2006 |
وصف مادي: | x, 278 p. : ill. (some col.) ; 24 cm. |
سلاسل: | Methods in molecular medicine Methods in molecular medicine |
مصطلحات موضوعية: | Congenital heart disease -- Molecular diagnosis., Congenital heart disease -- Genetic aspects., Heart -- Diseases -- Molecular diagnosis., Heart -- Diseases -- Genetic aspects., Molecular diagnosis., Heart Defects, Congenital -- diagnosis., Diagnostic Techniques, Cardiovascular., Heart Defects, Congenital -- genetics., Molecular Biology -- methods. |
ملاحظة حول المحتويات: | Genetics of cardiac septation defects and their pre-implantation diagnosis / Deborah A. McDermott, Craig T. Basson, and Cathy J. Hatcher -- Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome / Deborah A. Driscoll -- Mutation screening for the genes causing cardiac arrhythmias / Jeffrey A. Towbin -- The molecular genetics of Marfan syndrome / Paul Coucke, Petra Van Acker, and Anne De Paepe -- Mutation analysis of PTPN11 in Noonan syndrome by WAVE analysis / Navaratnam Elanko and Steve Jeffery -- Williams-Beuren syndrome / Lucy Osborne, Ann M. Joseph-George, and Stephen W. Scherer. Congenital heart disease: molecular diagnostics of supravalvular aortic stenosis / May Tassabehji and Zsolt Urban -- "Chip"-ping away at heart failure / J. David Barrans and Choong-Chin Liew -- Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia / Alex V. Postma, Zahurul A. Bhuiyan, and Hennie Bikker -- Mutation detection in tumor suppressor genes using archival tissue specimens / Aristotelis Astrinidis and Elizabeth Petri Henske -- Friedreich ataxia / Massimo Pandolfo. The cardiovascular manifestations of Alagille syndrome and JAG1 mutations / Elizabeth Goldmuntz, Elizabeth Moore, and Nancy Spinner -- Array analysis applied to malformed hearts: molecular dissection of tetralogy of fallot / Silke Sperling -- DNA mutational analysis in heterotaxy / Stephanie Ware -- Use of denaturing high performance liquid chromatography to detect mutations in pediatric cardiomyopathies / Amy J. Sehnert. |
Original Identifier: | ocm61479588 |
نوع الوثيقة: | Book |
اللغة: | English |
ردمك: | 978-1-58829-375-6 1-58829-375-0 |
حقوق: | This record is part of the Harvard Library Bibliographic Dataset, which is provided by the Harvard Library under its Bibliographic Dataset Use Terms and includes data made available by, among others, OCLC Online Computer Library Center, Inc. and the Library of Congress. |
ملاحظات: | Includes bibliographical references and index. |
رقم الأكسشن: | edshlc.009958580.4 |
قاعدة البيانات: | Harvard Library Bibliographic Dataset |
ردمك: | 9781588293756 1588293750 |
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