Mohamed ream (10 risultati)
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Da: preigu, Osnabrück, Germaniapreigu
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 51,75
EUR 70,00 spedizioneSpedito da Germania a U.S.A.Quantità: 5 disponibili
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 Osna…brück, mail[at]preigu[dot]de | Anbieter: preigu.
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Da: Mispah books, Redhill, SURRE, Regno UnitoMispah books
Contatta il venditoreVenditore con 4 stelleCondizione: Nuovo
EUR 199,27
EUR 29,14 spedizioneSpedito da Regno Unito a U.S.A.Quantità: 1 disponibili
paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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- Print on Demand
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 35,90
EUR 23,00 spedizioneSpedito da Germania a U.S.A.Quantità: 2 disponibili
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 s…ickle 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.
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Da: moluna, Greven, Germaniamoluna
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 31,27
EUR 48,99 spedizioneSpedito da Germania a U.S.A.Quantità: Più di 20 disponibili
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 Hema…tology theory and practical in b.
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- Print on Demand
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 59,90
EUR 23,00 spedizioneSpedito da Germania a U.S.A.Quantità: 2 disponibili
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.
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- Print on Demand
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 35,90
EUR 60,00 spedizioneSpedito da Germania a U.S.A.Quantità: 1 disponibili
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 sic…kle 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.
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- Print on Demand
Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 35,90
EUR 60,51 spedizioneSpedito da Germania a U.S.A.Quantità: 1 disponibili
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.
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- Print on Demand
Da: moluna, Greven, Germaniamoluna
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 49,17
EUR 48,99 spedizioneSpedito da Germania a U.S.A.Quantità: Più di 20 disponibili
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 Hem…atology. Main interests are Mole.
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- Print on Demand
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 59,90
EUR 60,00 spedizioneSpedito da Germania a U.S.A.Quantità: 1 disponibili
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 spec…ific 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.
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- Print on Demand
Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
EUR 59,90
EUR 60,90 spedizioneSpedito da Germania a U.S.A.Quantità: 1 disponibili
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 speci…fic 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.
