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1

Frederick, Hecht, ed. Fragile sites on human chromosomes. New York: Oxford University Press, 1985.

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2

B, Berch Daniel, Bender Bruce G, and American Association for the Advancement of Science. National Meeting, eds. Sex chromosome abnormalities and human behavior: Psychological studies. Boulder, Colo: Published by Westview Press for the American Association for the Advancement of Science, 1990.

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3

1926-, Hirschhorn Kurt, Paul Natalie W, and March of Dimes Birth Defects Foundation., eds. A guide to human chromosome defects. 3rd ed. White Plains, N.Y. (1275 Mamaroneck Ave., White Plains 10605): March of Dimes Birth Defects Foundation, 1992.

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4

Pai, G. Shashidhar. Handbook of chromosomal syndromes. New York: J. Wiley, 2003.

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5

G, Obe, and Natarajan A. T, eds. Chromosomal aberrations: Basic and applied aspects. Berlin: Springer-Verlag, 1990.

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6

G, Obe, and Natarajan A. T, eds. Chromosomal alterations: Origin and significance. Berlin: Springer-Verlag, 1994.

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7

S, Verma Ram, and Babu Arvind, eds. Human chromosomes: Principles and techniques. 2nd ed. New York: McGraw-Hill, 1995.

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8

F, Carter Ronald, ed. Genetic testing: Care, consent and liability. Hoboken, N.J: Wiley-Liss, 2006.

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9

universitet, Københavns, ed. Characterization of DNA polymorphisms on human chromosome 21 and their use in the study of unbalanced karyotypes, with special reference to nondisjunction in trisomy 21. Denmark]: Alma, 1996.

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10

A, Sandberg Avery, ed. The Y chromosome. New York: A.R. Liss, 1985.

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11

Therman, Eeva. Human chromosomes: Structure, behavior, effects. 2nd ed. New York: Springer-Verlag, 1985.

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12

A, Evans Jane, Hamerton John L, Robinson Arthur 1914-, and March of Dimes Birth Defects Foundation., eds. Children and young adults with sex chromosome aneuploidy: Follow-up, clinical, and molecular studies : proceedings of the 5th International Workshop on Sex Chromosome Anomalies held at Minaki, Ontario, Canada, June 7-10, 1989. New York: Wiley-Liss, 1991.

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13

Programme, United Nations Environment, International Labour Organisation, and World Health Organization, eds. Guidelines for the study of genetic effects in human populations. Geneva: World Health Organization, 1985.

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14

Méhes, Károly. A centroméraszétválás sorrendje: Akadémiai székfoglaló, 1991. március 12. Budapest: Akadémiai Kiadó, 1992.

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15

Frank, DeStefano, RTI International, and United States. Agency for Healthcare Research and Quality., eds. Infrastructure to monitor utilization and outcomes of gene-based applications: An assessment. Rockville, MD: U.S. Dept. of Heath and Human Services, Public Health Service, Agency for Healthcare Research and Quality, 2008.

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16

Verma, Ram S. Human chromosomes: Manual of basic techniques. New York: Pergamon Press, 1989.

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17

Verma, Ram S. Human chromosomes: Manual of basic techniques. Oxford: Pergamon, 1989.

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18

B, Cassidy Suzanne, North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders (1991 : Noordwijkerhout, Netherlands), eds. Prader-Willi syndrome and other chromosome 15q deletion disorders. Berlin: Springer-Verlag, 1992.

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19

Art, Daniel, ed. The Cytogenetics of mammalian autosomal rearrangements. New York: A.R. Liss, 1988.

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20

H, Nicolaides K., ed. Ultrasound markers for fetal chromosomal defects. New York: Parthenon Pub. Group, 1996.

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21

G, Shaffer Lisa, Slovak Marilyn L, and Campbell Lynda J, eds. ISCN 2009: An international system for human cytogenetic nomenclature (2009). Basel: Karger, 2009.

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22

Commission, European, Organisation for Economic Co-operation and Development., and Genetic Testing : Policy Issues for the New Millennium (2000 : Vienna, Austria), eds. Genetic testing: Policy issues for the new millennium. Paris, France: Organisation for Economic Co-operation and Development, 2000.

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23

Judd, Sandra J. Genetic disorders sourcebook: Basic consumer health information about heritable disorders, including disorders resulting from abnormalities in specific genes ... 4th ed. Detroit, MI: Omnigraphics, 2010.

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24

J, Judd Sandra, ed. Genetic disorders sourcebook: Basic consumer health information about heritable disorders, including disorders resulting from abnormalities in specific genes ... 4th ed. Detroit, MI: Omnigraphics, 2009.

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25

Great Britain. Advisory Committee on Genetic Testing. Report on genetic testing for late onset disorders: September 1998. London: Health Departments of the United Kingdom, 1998.

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26

Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health, ed. Value of genetic and genomic technologies: Workshop summary. Washington, D.C: National Academies Press, 2010.

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27

G, Harnden D., and Klinger Harold P. 1929-, eds. An international system for human cytogenetic nomenclature (1985): ISCN (1985) : report of the Standing Committee on Human Cytogenetic Nomenclature. Basel: S. Karger, 1985.

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28

Berch, Daniel B., and Bruce G. Bender. Sex Chromosome Abnormalities and Human Behavior: Psychological Studies. Taylor & Francis Group, 2019.

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29

Berch, Daniel B., and Bruce G. Bender. Sex Chromosome Abnormalities and Human Behavior: Psychological Studies. Taylor & Francis Group, 2019.

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30

Berch, Daniel B., and Bruce G. Bender. Sex Chromosome Abnormalities and Human Behavior: Psychological Studies. Taylor & Francis Group, 2019.

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31

Berch, Daniel B., and Bruce G. Bender. Sex Chromosome Abnormalities and Human Behavior: Psychological Studies. Taylor & Francis Group, 2019.

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32

Berch, Daniel B., and Bruce G. Bender. Sex Chromosome Abnormalities and Human Behavior. Edited by Daniel B. Berch and Bruce G. Bender. CRC Press, 2019. http://dx.doi.org/10.1201/9780429305870.

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33

Sutherland, Grant R., and R. J. McKinlay Gardner. Chromosome Abnormalities and Genetic Counseling. Oxford University Press, 2012.

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34

The Y Chromosome, Part A. Wiley-Liss, 1985.

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35

Miller, Orlando J. Human Chromosomes. Island Press, 2000.

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36

Miller, Orlando J. Human Chromosomes. Springer, 2000.

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37

Human Chromosomes. Island Press, 1995.

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38

Miller, Orlando J. Human Chromosomes. 4th ed. Springer, 2000.

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39

Miller, Orlando J. Human Chromosomes. Springer London, Limited, 2011.

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40

Human Chromosomes. Island Press, 1989.

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41

Lundsteen, Claes. Automation of Cytogenetics. Springer, 2012.

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42

Jalal, Syed M. Atlas of whole chromosome paint probes: Normal patterns and utility for abnormal cases. Mayo foundation for Medical Education and Research, 1996.

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43

Turleau, Catherine, and Jean de Grouchy. Atlas des maladies chromosomiques. Elsevier France, 1988.

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44

Liehr, Thomas. Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations in Genetics and Counseling. Elsevier Science & Technology Books, 2013.

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45

Wyatt, Sally, Susan Kelly, and Anna Harris. Cybergenetics. Taylor & Francis Group, 2018.

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46

Mendelian Inheritance in Man. July / Dec 94 Issue. The Johns Hopkins University Press, 1996.

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47

Human Chromosomes: Structure, Behavior, Effects. Springer London, Limited, 2012.

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48

Human Chromosomes: Structure, Behavior, Effects. Springer London, Limited, 2012.

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49

Pai, G. Shashidhar, Raymond C. Jr Lewandowski, and Digamber S. Borgaonkar. Handbook of Chromosomal Syndromes. Wiley-Liss, 2002.

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50

Gardner, R. J. McKinlay, and David J. Amor. Gardner and Sutherland’s Chromosome Abnormalities and Genetic Counseling. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199329007.001.0001.

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Abstract:
Medical geneticists and genetic counselors regularly see families attending the genetic counseling clinic with questions about chromosome abnormalities. These families may themselves have had a child affected with a chromosome condition; or, there may have been a history elsewhere in the family. The presentation may have been due to infertility or reproductive loss. Questions may include the following: What is known about this condition? What caused this to happen? Is it likely to happen again? If so, is there a way to prevent it from happening again? The power of molecular approaches to chromosome analysis, coming to be routinely available in this second decade of the twenty-first century, has brought to our knowledge many new “chromosomal syndromes” to add alongside those long known from the days of classical cytogenetics. This new knowledge has increased our ability to answer the questions that families may have; but equally, it has raised challenges in interpretation, as molecular karyotyping has revealed more complexity in the way the human genome is constructed. This book distils the knowledge that has evolved in recent and olden times, and it presents the information in a way that will be helpful to the practitioner. In particular, the risks of recurrence, or of occurrence, of a particular chromosome disorder are clearly set forth. The application of chromosomal knowledge to reproductive conditions, both diagnostically and in management, is rehearsed.
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