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OverviewFanconi anemia (FA) is autosomal recessive disorder. Molecular study of FA revealed that there are 15 genetic subtypes groups with FANCA gene being the most frequent. The rate of successful cytogenetic cell culture varies with the specific type of disease. Many factors can affect the cytogenetic cell culture and the successful appearance of metaphase. The determination of the amount of blood uses in cytogenetic cell culture is important to obtain excellent metaphase. The highlight of the book lies on identification and diagnosis of Fanconi anemia among aplastic anemia patients with Special emphasis on identification of FANCA gene mutations. The book also improves the chromosomal breakage test and reduces lymphocyte cell culture failure. The book is extremely useful for medical laboratory students and researchers working in hematology. Postgraduate students would find this book informative and handy. Full Product DetailsAuthor: Ream Mohamed , Abdel Rahim Muddathir , Imad Fadl- ElmulaPublisher: Scholars' Press Imprint: Scholars' Press Dimensions: Width: 15.20cm , Height: 0.70cm , Length: 22.90cm Weight: 0.168kg ISBN: 9783639718331ISBN 10: 363971833 Pages: 108 Publication Date: 10 June 2014 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In stock  We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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