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1

Rees, Sally Anne. Fluorescence in situ hybridisation (FISH) to determine aneuploidy for chromosomes 1 and 12 in the normal male germ-line and in men exposed to radiation. Birmingham: University of Birmingham, 1997.

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2

Bridger, Joanna M., and Emanuela V. Volpi, eds. Fluorescence in situ Hybridization (FISH). Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-789-1.

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3

Liehr, Thomas, ed. Fluorescence In Situ Hybridization (FISH). Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-52959-1.

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4

Liehr, Thomas. Fluorescence In Situ Hybridization (FISH) — Application Guide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.

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5

Liehr, Thomas, ed. Fluorescence In Situ Hybridization (FISH) — Application Guide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-70581-9.

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6

Fluorescence in situ hybridization (FISH): Protocols and applications. New York, NY: Humana Press, 2010.

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7

Azevedo, Nuno F., and Carina Almeida, eds. Fluorescence In-Situ Hybridization (FISH) for Microbial Cells. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1115-9.

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8

Bysouth, James Peter Norman. Physical mapping of 45S and 5S rDNA repetitive sequences to mitotic chromosomes of Brassica species by fluorescence in situ hybridisation. Birmingham: University of Birmingham, 2003.

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9

O'Keeffe, Christine. Analysis of the initiation and progression of homologous chromosome pairing at meiosis in the female mouse using fluorescence in situ hybridisation. Birmingham: University of Birmingham, 1997.

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10

FISH handbook for biological wastewater treatment: Identification and quantification of microorganisms in activated sludge and biofilms by FISH. London: New York, 2009.

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11

1959-, Rautenstrauss Bernd W., and Liehr Thomas 1965-, eds. FISH technology. Berlin: Springer, 2002.

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12

1944-, Beatty Barbara, Mai Sabine, and Squire Jeremy 1950-, eds. FISH: A practical approach. Oxford: Oxford University Press, 2002.

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13

(Editor), Bernd W. Rautenstrauß, and Thomas Liehr (Editor), eds. FISH Technology (Springer Lab Manuals). Springer, 2002.

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14

Cytogenetics, FISH and Molecular Testing in Hematologic Malignancies. Informa Healthcare, 2008.

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15

Zneimer, Susan Mahler. Cytogenetic Abnormalities: Chromosomal, FISH, and Microarray-Based Clinical Reporting and Interpretation of Result. Wiley & Sons, Incorporated, John, 2014.

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16

Zneimer, Susan Mahler. Cytogenetic Abnormalities: Chromosomal, FISH, and Microarray-Based Clinical Reporting and Interpretation of Result. Wiley & Sons, Incorporated, John, 2014.

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17

Zneimer, Susan Mahler. Cytogenetic Abnormalities: Chromosomal, FISH, and Microarray-Based Clinical Reporting and Interpretation of Result. Wiley & Sons, Incorporated, John, 2014.

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18

Mathiesen, Amber, and Kali Roy. Prenatal Diagnosis. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190681098.003.0004.

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Prenatal diagnosis is the term used to describe a set of tests that are designed to determine whether a specific genetic condition is present in a fetus. This chapter provides a detailed description of procedures as well as the types of testing options available for prenatal diagnosis. The two techniques for prenatal diagnosis, amniocentesis and chorionic villus sampling, are described in detail, including their procedures, risks, limitations, and their use in twin gestations. The prenatal diagnosis testing options are also described in detail, including karyotype, fluorescence in situ hybridization (FISH), microarray, molecular testing, and alpha-fetoprotein (AFP) and acetylcholinesterase (AChE) level testing. The chapter also includes images of karyotype, FISH, and microarray test results, and it also reviews the indications for prenatal diagnostic testing.
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