mohamed ream (11 risultati)

Taschenbuch. Condizione: Neu. Evaluation of sickling test in diagnosis of hemoglobin S (HbS) | Ream Mohamed (u. a.) | Taschenbuch | 56 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659622113 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Taschenbuch. Condizione: Neu. Molecular Characterizations of Fanconi Anemia Type A (FANCA) gene | Genetic heterogeneity of FANCA gene | Ream Mohamed (u. a.) | Taschenbuch | 108 S. | Englisch | 2014 | Scholars' Press | EAN 9783639718331 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Sickle cell disease is one of the most causes of morbidity and mortality among children.Sickling test is still the mainstay tool for diagnosis of Hb S ,the highlight of the book lies on evaluation of sickling test in diagnosis of sickle cell disease by knowing of sensitivity and specificity of sikling test in compare with hemoglobin electrophoresis as standard method. Determination of sensitivity and specificity of scikling test will helps to choose the appropriate method for diagnosis of sickle cell disease. Extremely useful for medical laboratory students and researchers working in hematology. 56 pp. Englisch.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Mohamed ReamDr. Ream Elzain is an Assistant Professor at department of Hematology at present in Faculty of medicine and health sciences, University of Kordofan, El-Obeid, Sudan. Dr. Ream, teaching Hematology theory and practical in b.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Fanconi 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. 108 pp. Englisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -¿ Sickle cell disease is one of the most causes of morbidity and mortality among children.Sickling test is still the mainstay tool for diagnosis of Hb S ,the highlight of the book lies on evaluation of sickling test in diagnosis of sickle cell disease by knowing of sensitivity and specificity of sikling test in compare with hemoglobin electrophoresis as standard method. \* Determination of sensitivity and specificity of scikling test will helps to choose the appropriate method for diagnosis of sickle cell disease. ¿Extremely useful for medical laboratory students and researchers working in hematology.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 56 pp. Englisch.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Sickle cell disease is one of the most causes of morbidity and mortality among children.Sickling test is still the mainstay tool for diagnosis of Hb S ,the highlight of the book lies on evaluation of sickling test in diagnosis of sickle cell disease by knowing of sensitivity and specificity of sikling test in compare with hemoglobin electrophoresis as standard method. Determination of sensitivity and specificity of scikling test will helps to choose the appropriate method for diagnosis of sickle cell disease. Extremely useful for medical laboratory students and researchers working in hematology.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Mohamed ReamReam Elzain is an Assistant Professor at department of Hematology at present in Faculty of medicine and health sciences, University of Kordofan, El-Obeid, Sudan. Having PhD in Molecular Hematology. Main interests are Mole.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Fanconi 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.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 108 pp. Englisch.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Fanconi 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.