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Books on the topic 'Chromosome polymorphism'

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Published: 4 June 2021
Last updated: 25 July 2024

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1

1939-, Wyandt Herman Edwin, and Tonk Vijay S, eds. Atlas of human chromosome heteromorphisms. Dordrecht: Kluwer Academic Publishers, 2003.

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2

Wyandt, Herman E., and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism and Polymorphism. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-0896-9.

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3

Wyandt, Herman E. Human Chromosome Variation: Heteromorphism and Polymorphism. Dordrecht: Springer Science+Business Media B.V., 2012.

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4

Wyandt, Herman E., Golder N. Wilson, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3035-2.

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5

Krimbas, Costas B. Drosophila subobscura: Biology, genetics, and inversion polymorphism. Hamburg: Kovač, 1993.

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6

University), National Seminar on Cytopolymorphism in Plants (1989 Annamalai. Proceedings of the National Seminar on Cytopolymorphism in Plants, 25th-27th February 1989. Annamalai Nagar: Annamalai University, 1991.

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7

R, Taylor G., ed. Laboratory methods for the detection of mutations and polymorphisms in DNA. Boca Raton: CRC Press, 1997.

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8

Ellegren, Hans. Genome analysis with microsatellite markers. Uppsala: Dept. of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 1993.

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9

Single nucleotide polymorphisms: Methods and protocols. 2nd ed. New York: Humana, 2009.

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10

Atlas of human chromosome heteromorphisms. Dordrecht: Kluwer Academic·, 2002.

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11

Drosophila inversion polymorphism. Boca Raton, Fla: CRC Press, 1992.

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12

Wilson, Golder N., Herman E. Wyandt, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Springer, 2017.

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13

Wilson, Golder N., Herman E. Wyandt, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Springer, 2018.

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14

1956-, Kwok Pui-Yan, ed. Single nucleotide polymorphisms: Methods and protocols. Totowa, N.J: Humana Press, 2003.

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15

India, Anthropological Survey Of, and D. N. A. Polymorphism DNA Polymorphism Consortium. Genomic Diversity in People of India: Focus on MtDNA and y-Chromosome Polymorphism. Springer Singapore Pte. Limited, 2021.

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16

India, Anthropological Survey Of, and D. N. A. Polymorphism DNA Polymorphism Consortium. Genomic Diversity in People of India: Focus on MtDNA and y-Chromosome Polymorphism. Springer, 2022.

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17

Kwok, Pui-Yan. Single Nucleotide Polymorphisms: Methods and Protocols (Methods in Molecular Biology). Humana Press, 2002.

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18

Komar, Anton A. Single Nucleotide Polymorphisms: Methods and Protocols. Humana Press, 2012.

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19

Clinical Cytogenetics, An Issue of Clinics in Laboratory Medicine. Saunders, 2012.

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20

Divan, Aysha, and Janice A. Royds. 2. DNA. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198723882.003.0002.

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Another significant milestone was the publication in 2003 of the complete sequence of the human genome—the entire DNA contained within the forty-six chromosomes located in the nucleus of each human somatic (body) cell. Once this was published, further worldwide projects were launched to work out what the functions of these genes and other regions of the genome actually were. ‘DNA’ outlines the components of the human genome and their organization; DNA replication; mutations and correction mechanisms; polymorphisms; and new DNA technologies, including gene cloning, the polymerase chain reaction, and sequencing methods. Finally, bioinformatics and the subsequent issues of privacy and how this information could be used are discussed.
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21

Weihbrecht, Sebastian Bernd. Assoziationen zwischen Polymorphismen im ˜Topoisomerase-II-α-Gen œ[Topoisomerase-II-alpha-Gen] mit der Länge des HER2-Amplikons suf Chromosom 17: Implikationen für Mechanismen der Genamplifikation und die Prognose bei Mammkarzinompatientinnen. 2010.

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22

Vermeulen, Roel, Douglas A. Bell, Dean P. Jones, Montserrat Garcia-Closas, Avrum Spira, Teresa W. Wang, Martyn T. Smith, Qing Lan, and Nathaniel Rothman. Application of Biomarkers in Cancer Epidemiology. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0006.

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Advancements in OMICs are now enabling investigators to explore comprehensively the biological consequences of exogenous and endogenous exposures by detecting molecular signatures of exposure, early signs of adverse biological effects, preclinical disease, and molecularly defined cancer subtypes. These new technologies have proven invaluable for assembling a comprehensive portrait of human exposure, health, and disease. This includes hypothesis-driven biomarkers, as well as platforms that can agnostically analyze entire biologic processes and “compartments,” including the measurement of small molecules (metabolomics), DNA polymorphisms and rarer inherited variants (genomics), methylation and microRNA (epigenomics), chromosome-wide alterations, mRNA (transcriptomics), proteins (proteomics), and the microbiome (microbiomics). Although the implementation of these technologies in epidemiologic studies has already shown great promise, some challenges of particular importance must be addressed. Non-genetic OMIC markers vary over time due to both random variation and physiologic changes. Therefore, there is an urgent need for cohorts to collect repeat biological samples over time.
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23

Weihbrecht, Sebastian Bernd. Assoziationen zwischen Polymorphismen im ˜Topoisomerase-II-α-Gen œ[Topoisomerase-II-alpha-Gen] mit der Länge des HER2-Amplikons auf Chromosom 17: Implikationen für Mechanismen der Genamplifikation und die Prognose bei Mammakarzinompatientinnen. 2010.

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24

Samuels, Jack, Marco A. Grados, Elizabeth Planalp, and O. Joseph Bienvenu. Genetic Understanding of OCD and Spectrum Disorders. Edited by Gail Steketee. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780195376210.013.0025.

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This chapter reviews the evidence for the genetic etiology of OCD and spectrum conditions. A genetic basis is supported by the familial aggregation of OCD; evidence for involvement of genes of major effect in segregation analyses; and higher concordance for OCD in identical than non-identical twins. Recent studies also support linkage of OCD to specific chromosomal regions and association of OCD with specific genetic polymorphisms. However, specific genes causing OCD have not yet been firmly established. The search for genes is complicated by the clinical and etiologic heterogeneity of OCD, as well as the possibility of gene–gene and gene–environmental interactions. Despite this complexity, developments in molecular and statistical genetics, and further refinement of the phenotype hold promise for further deepening our genetic understanding of OCD and spectrum disorders in the coming decade.
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25

Rabinow, Paul. French DNA: Trouble in Purgatory. University Of Chicago Press, 2002.

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26

Rabinow, Paul. French DNA: Trouble in Purgatory. University Of Chicago Press, 1999.

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