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1

Bhat, Tariq Ahmad, and Aijaz Ahmad Wani, eds. Chromosome Structure and Aberrations. New Delhi: Springer India, 2017. http://dx.doi.org/10.1007/978-81-322-3673-3.

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2

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

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3

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

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4

1963-, Johansson Bertil, and Mertens Fredrik, eds. Catalog of chromosome aberrations in cancer. 5th ed. New York: Wiley-Liss, 1994.

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5

Felix, Mitelman, ed. Catalog of chromosome aberrations in cancer. 2nd ed. New York: Liss, 1985.

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6

T, Leyden Guy, ed. Genetic translocations and other chromosome aberrations. New York: Nova Biomedical Books, 2008.

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7

György, Fekete. Congenital chromosome aberrations and tumour predisposition. Budapest: Adadémiai Kiadó, 1990.

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8

Bullerdiek, J., and S. Bartnitzke, eds. Chromosome 12 Aberrations in Human Solid Tumors. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-06255-5.

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9

K, Vig Baldev, and NATO Advanced Research Workshop on Chromosome Segregation and Aneuploidy (1992 : Aghia Pelagia, Greece), eds. Chromosome segregation and aneuploidy. Berlin: Springer-Verlag, 1993.

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10

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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11

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

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12

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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13

Jörn, Bullerdiek, and Bartnitzke S. 1955-, eds. Chromosome 12 aberrations in human solid tumors: Cytogenetics and molecular genetics. Berlin: Springer-Verlag, 1994.

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14

Great Britain. Human Fertilisation & Embryology Authority. Report of the Human Fertilisation and Embryology Authority annual conference, Monday 15 December 1997, Royal College of Physicians, London. London]: [The Authority], 1997.

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15

N, Weingarten Cynthia, and Jefferson Sally E, eds. Sex chromosomes: Genetics, abnormalities, and disorders. Hauppauge, NY: Nova Science Publishers, 2009.

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16

E, Antonarakis Stylianos, ed. Genomic imprinting and uniparental disomy in medicine: Clinical and molecular aspects. New York: Wiley-Liss, 2002.

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17

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

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18

Hamta, Ahmad. The BDII rat model of endometrial cancer: Molecular analysis of genetic and cytogenetic aberrations. Göteborg: Department of Cell and Molecular Biology-Genetics, Lundberg Institute, Göteborg University, 2006.

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19

Hamta, Ahmad. The BDII rat model of endometrial cancer: Molecular analysis of genetic and cytogenetic aberrations. Göteborg: Department of Cell and Molecular Biology-Genetics, Lundberg Institute, Göteborg University, 2006.

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20

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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21

Warburton, Dorothy. Chromosome anomalies and prenatal development: An atlas. New York: Oxford University Press, 1990.

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22

M, Byrne Julianne, and Canki Nina, eds. Chromosome anomalies and prenatal development: An atlas. New York: Oxford University Press, 1991.

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23

G, Ratcliffe Shirley, Paul Natalie W, and March of Dimes Birth Defects Foundation., eds. Prospective studies on children with sex chromosome aneuploidy. New York: Liss, 1986.

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24

1934-, Holtzman Neil A., and Watson Michael S, eds. Promoting safe and effective genetic testing in the United States: Final report of the Task Force on Genetic Testing. Baltimore: Johns Hopkins University Press, 1998.

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25

Motoi, Ishidate, ed. Data book of chromosomal aberration test in vitro. Amsterdam: Elsevier, 1988.

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26

Kuo, Michael Jeo-Ming. Aberrations of chromosome arms 5q and 8p in squamous cell carcinomas of the head and neck. Birmingham: University of Birmingham, 1998.

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27

Karen, Bellenir, ed. Genetic disorders sourcebook: Basic information about heritable diseases and disorders such as Down syndrome, PKU, hemophilia, Von Willebrand disease, Gaucher disease, Tay-Sachs disease, and sickle cell disease ... Detroit, MI: Omnigraphics, 1996.

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28

Seiichiro, Fujimoto, ed. Clinical application of serum alpha-fetoprotein microheterogeneity. Sapporo, Japan: Hokkaido University Graduate School of Medicine, 2001.

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29

Bellenir, Karen. Genetic disorders sourcebook: Basic consumer health information about hereditary diseases and disorders, including facts about the human genome, genetic inheritance patterns, disorders associated with specific genes ... 3rd ed. Detroit, Mich: Omnigraphics, 2004.

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30

Kathy, Massimini, ed. Genetic disorders sourcebook: Basic consumer health information about hereditary diseases and disorders, including cystic fibrosis, Down syndrome ... 2nd ed. Detroit, MI: Omnigraphics, 2000.

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31

1946-, Oostra Ben A., ed. Trinucleotide diseases and instability. Berlin: Springer, 1998.

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32

E, Davies K., ed. The Fragile X syndrome. Oxford: Oxford University Press, 1989.

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33

Reinhard, Becher, Sandberg Avery A, Schmidt C. G, Westdeutsches Tumorzentrum (Essen Germany), and International Symposium on "Chromosomes in Hematology" (1986 : Münster in Westfalen, Germany), eds. Chromosomes in hematology: International symposium of the West-German Cancer Center Essen, Münster 1986. München: W. Zuckschwerdt Verlag, 1986.

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34

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

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35

M, Optiz John, Paul Natalie W, and March of Dimes Birth Defects Foundation., eds. Blastogenesis: Normal and abormal : proceedings of the Second International Workshop on Fetal Genetic Pathology, held at Big Sky, Montana, 12-16 October 1991. New York: Wiley-Liss, 1993.

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36

1935-1994, Axelrod David, Randolph Linda A, and Rouse Ronald L, eds. New York State genetic reimbursement study. Albany, N.Y: New York State Department of Health, 1988.

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37

Kingston, Helen M. ABC of clinical genetics. London: British Medical Association, 1989.

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38

1952-, Ludwig W. D., and Thiel Eckhard 1944-, eds. Recent advances in cell biology of acute leukemia: Impact on clinical diagnosis and therapy. Berlin: Springer-Verlag, 1993.

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39

Bhat, Tariq Ahmad, and Aijaz Ahmad Wani. Chromosome Structure and Aberrations. Springer, 2017.

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40

Bhat, Tariq Ahmad, and Aijaz Ahmad Wani. Chromosome Structure and Aberrations. Springer, 2018.

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41

Catalog of chromosome aberrations in cancer. 3rd ed. New York: Liss, 1988.

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42

Catalog of chromosome aberrations in cancer. 4th ed. New York: Wiley-Liss, 1991.

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43

Bullerdiek, Jorn, and S. Bartnitzke. Chromosome 12 Aberrations in Human Solid Tumors: Cytogenetics and Molecular Genetics. Springer-Verlag Telos, 1994.

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44

Schinzel, Albert. Catalogue of Unbalanced Chromosome Aberrations in Man. de Gruyter GmbH, Walter, 2020.

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45

Bullerdiek, Jörn. Chromosome 12 Aberrations in Human Solid Tumors. Springer, 2013.

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46

Catalogue of Unbalanced Chromosome Aberrations in Man. 2nd ed. Walter de Gruyter, 2001.

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47

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

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48

Vig, Baldev K. Chromosome Segregation and Aneuploidy. Springer London, Limited, 2013.

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49

Vig, Baldev K. Chromosome Segregation and Aneuploidy. Springer, 2012.

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50

Vig, Baldev K. Chromosome Segregation and Aneuploidy. Springer London, Limited, 2012.

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