Cytogenetics - Couverture souple

Mallikarjunaiah, Shanthala ; Karunyaa R, Jyoti

Couverture souple

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

Editeur : LAP Lambert Academic Publishing, 2025

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�diteur: LAP Lambert Academic Publishing
Date d'�dition: 2025
Langue: anglais
ISBN 10: 6208470234
ISBN 13: 9786208470234
Reliure: Broch�
Nombre de pages: 80
Coordonn�es du fabricant: non disponible
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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP LAMBERT Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP LAMBERT Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics (Paperback)

Shanthala Mallikarjunaiah

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Paperback. Etat : new. Paperback. Acute myeloid leukemia (AML) is a category of diseases with a common aggressive clinical presentation but with a poor prognosis and management that is dependent upon the underlying genetic characteristics of the neoplasm. Genetic analysis of AML is essential, and conventional karyotyping is the key factor in diagnosis and management of AML. In this study, 65952 cases were studied from the data, 251 males (63.87%) and 142 females (36.13%). The range of age in this study was 2 months to 87 years. The maximum chromosomal abnormality was observed in males compared to females, median age of 31 years. Individual karyotypes showed that total 23 types of rare cytogenetic abnormalities were recorded. The analysis of AML data showed that incidence of ph+ve chromosome, complex karyotypes, tetraploid/near tetraploid (T/NT), t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12)(p15.2;q24.11), high hyperploidy, >=49 chromosomes; tetraploidy (4n = 92 chromosomes) are marker karyotype, which were of significance. del Y or X, 9,7; Abn19q13; Trisomy22, Core binding factor (CBF) (+ve AML). The highest % incidence of individual rare abnormalities in AML patients is t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12). This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. N� de r�f. du vendeur 9786208470234

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CYTOGENETICS

Shanthala Mallikarjunaiah

Edit� par Omniscriptum, LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Acute myeloid leukemia (AML) is a category of diseases with a common aggressive clinical presentation but with a poor prognosis and management that is dependent upon the underlying genetic characteristics of the neoplasm. Genetic analysis of AML is essential, and conventional karyotyping is the key factor in diagnosis and management of AML. In this study, 65952 cases were studied from the data, 251 males (63.87%) and 142 females (36.13%). The range of age in this study was 2 months to 87 years. The maximum chromosomal abnormality was observed in males compared to females, median age of 31 years. Individual karyotypes showed that total 23 types of rare cytogenetic abnormalities were recorded. The analysis of AML data showed that incidence of ph+ve chromosome, complex karyotypes, tetraploid/near tetraploid (T/NT), t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12)(p15.2;q24.11), high hyperploidy, 49 chromosomes; tetraploidy (4n = 92 chromosomes) are marker karyotype, which were of significance. del Y or X, 9,7; Abn19q13; Trisomy22, Core binding factor (CBF) (+ve AML). The highest % incidence of individual rare abnormalities in AML patients is t(1;2)(p35;p22),t(1;3)(p36.2;p26.2) t(10;12). 80 pp. Englisch. N� de r�f. du vendeur 9786208470234

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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics

Mallikarjunaiah, Shanthala; Karunyaa R, Jyoti

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Cytogenetics (Paperback)

Shanthala Mallikarjunaiah

Edit� par LAP Lambert Academic Publishing, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Paperback. Etat : new. Paperback. Acute myeloid leukemia (AML) is a category of diseases with a common aggressive clinical presentation but with a poor prognosis and management that is dependent upon the underlying genetic characteristics of the neoplasm. Genetic analysis of AML is essential, and conventional karyotyping is the key factor in diagnosis and management of AML. In this study, 65952 cases were studied from the data, 251 males (63.87%) and 142 females (36.13%). The range of age in this study was 2 months to 87 years. The maximum chromosomal abnormality was observed in males compared to females, median age of 31 years. Individual karyotypes showed that total 23 types of rare cytogenetic abnormalities were recorded. The analysis of AML data showed that incidence of ph+ve chromosome, complex karyotypes, tetraploid/near tetraploid (T/NT), t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12)(p15.2;q24.11), high hyperploidy, >=49 chromosomes; tetraploidy (4n = 92 chromosomes) are marker karyotype, which were of significance. del Y or X, 9,7; Abn19q13; Trisomy22, Core binding factor (CBF) (+ve AML). The highest % incidence of individual rare abnormalities in AML patients is t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12). This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. N� de r�f. du vendeur 9786208470234

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CYTOGENETICS

Shanthala Mallikarjunaiah

Edit� par LAP LAMBERT Academic Publishing Okt 2025, 2025

ISBN 10 : 6208470234 ISBN 13 : 9786208470234

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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Acute myeloid leukemia (AML) is a category of diseases with a common aggressive clinical presentation but with a poor prognosis and management that is dependent upon the underlying genetic characteristics of the neoplasm. Genetic analysis of AML is essential, and conventional karyotyping is the key factor in diagnosis and management of AML. In this study, 65952 cases were studied from the data, 251 males (63.87%) and 142 females (36.13%). The range of age in this study was 2 months to 87 years. The maximum chromosomal abnormality was observed in males compared to females, median age of 31 years. Individual karyotypes showed that total 23 types of rare cytogenetic abnormalities were recorded. The analysis of AML data showed that incidence of ph+ve chromosome, complex karyotypes, tetraploid/near tetraploid (T/NT), t(1;2)(p35;p22), t(1;3)(p36.2;p26.2) t(10;12)(p15.2;q24.11), high hyperploidy, �49 chromosomes; tetraploidy (4n = 92 chromosomes) are marker karyotype, which were of significance. del Y or X, 9,7; Abn19q13; Trisomy22, Core binding factor (CBF) (+ve AML). The highest % incidence of individual rare abnormalities in AML patients is t(1;2)(p35;p22),t(1;3)(p36.2;p26.2) t(10;12).VDM Verlag, Dudweiler Landstra�e 99, 66123 Saarbr�cken 80 pp. Englisch. N� de r�f. du vendeur 9786208470234

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