Description

Now in its second edition, this atlas serves as an easy-to-use diagnostic guide for the analysis of the human karyotype.

Split in four parts, it starts with a comprehensive introduction covering the molecular cytogenetic basics, the role of ethic committees and international quality control in the field of diagnostics. The main parts II and III show the spectrum of different types of chromosomal abnormalities by a combination of karyogram and ideogram. They compare the significance of different banding techniques, give the karyotype formula and describe morphological peculiarities of each case presented. The final part provides a detailed description of non-coding DNA variants and focuses on potential problems in the detection of aberrations. It also mentions necessary additional investigations and peculiarities to be considered when counselling carriers of a chromosomal aberration or their relatives.

Given its comprehensive scope and practical approach, this atlas is an indispensable resource for researchers, clinicians and practitioners working in the field of cytogenetics and clinical genetics.

Human Chromosome Atlas: Introduction to Diagnostics of Structural Aberrations

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£119.99

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Hardback by Claudia Behrend , Javad Karimzad Hagh

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Short Description:

Now in its second edition, this atlas serves as an easy-to-use diagnostic guide for the analysis of the human karyotype.... Read more

    Publisher: Springer International Publishing AG
    Publication Date: 01/03/2023
    ISBN13: 9783031105876, 978-3031105876
    ISBN10: 3031105877

    Number of Pages: 388

    Non Fiction , Education

    Description

    Now in its second edition, this atlas serves as an easy-to-use diagnostic guide for the analysis of the human karyotype.

    Split in four parts, it starts with a comprehensive introduction covering the molecular cytogenetic basics, the role of ethic committees and international quality control in the field of diagnostics. The main parts II and III show the spectrum of different types of chromosomal abnormalities by a combination of karyogram and ideogram. They compare the significance of different banding techniques, give the karyotype formula and describe morphological peculiarities of each case presented. The final part provides a detailed description of non-coding DNA variants and focuses on potential problems in the detection of aberrations. It also mentions necessary additional investigations and peculiarities to be considered when counselling carriers of a chromosomal aberration or their relatives.

    Given its comprehensive scope and practical approach, this atlas is an indispensable resource for researchers, clinicians and practitioners working in the field of cytogenetics and clinical genetics.

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