Books on the topic 'X and Y chromosomes'

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

Miller, James R. X-linked traits: A catalog of loci in nonhuman mammals. Cambridge: Cambridge University Press, 1990.

Sado, Takashi, ed. X-Chromosome Inactivation. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8766-5.

Grön, Mathias. Effects of human X and Y chromosomes on oral and craniofacial morphology. Oulu, Finland: Oulun Yliopisto, 1999.

The X in sex: How the X chromosome controls our lives. Cambridge, Mass: Harvard University Press, 2003.

Letsche, Curt. Chromosom X: Eine keineswegs phantastische Geschichte. Berlin: Spotless, 1994.

E, Schwartz Charles, and Schroer Richard J, eds. X-linked mental retardation. New York: Oxford University Press, 2000.

Veenema, Henk. Clinical, cytogenetic and molecular aspects of the fragile-X syndrome. Amsterdam/Haarlem: Uitgeverij Thesis, 1989.

McKusick, Victor A. Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. 9th ed. Baltimore: Johns Hopkins University Press, 1990.

Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive, and x-linked phenotypes. 7th ed. Baltimore: Johns Hopkins University Press, 1986.

A, Francomano Clair, and Antonarakis Stylianos E, eds. Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. Baltimore: Johns Hopkins University Press, 1992.

Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. 8th ed. Baltimore: Johns Hopkins University Press, 1988.

Tassone, Flora, and Elizabeth M. Berry-Kravis. Fragile X-associated tremor ataxia syndrome (FXTAS). New York: Springer, 2010.

Spotswood, Hugh Timothy. Histone modification and the epigenetics of X chromosome inactivation. Birmingham: University of Birminghm, 2002.

Michalickova, Katerina. X-chromosome inactivation in females with deletions at Xq27-q28. Ottawa: National Library of Canada, 1996.

M, Optiz John, and Neri Giovanni, eds. X-linked mental retardation 3: Proceedings of the Third International Workshop on Fragile X and X-linked Mental Retardation held in Troina, Italy, September 13-16, 1987. New York: Liss, 1988.

M, Opitz John, Reynolds James F, and Spano Lavelle M, eds. X-linked mental retardation 2: Proceedings of the Second International Workshop on Fragile X and X-linked Mental Retardation held on Dunk Island, Australia, August 20-23, 1985. New York: Liss, 1986.

Lehrke, Robert Gordon. Sex linkage of intelligence: The X-factor. Westport, Conn: Praeger, 1997.

Postel-Vinay, Olivier. La revanche du chromosome X: Enquête sur les origines et le devenir du féminin. Paris: JC Lattès, 2007.

M, Coates Christine, ed. Living with my X: True story of one man and a rogue chromosome. Cape Town, South Africa: Zebra Press, 2010.

Females are mosaics: X inactivation and sex differences in disease. New York, NY: Oxford University Press, 2006.

M, Willey Ann, and Murphy Patricia D, eds. Fragile X--cancer cytogenetics: Proceedings of the 1989 Albany Birth Defects Symposium XX, held in Albany, New York, October 16-17, 1989. New York: Wiley-Liss, 1991.

Bate, Rachael. Mapping and gene identification within the Ids to Dmd region of the mouse X chromosome. Oxford: Oxford Brookes University, 2002.

Mastro, Richard Giulio Del. The human genome: Mapping the X-chromosome and the molecular analysis of selected genetic diseases. Birmingham: University of Birmingham, 1991.

The XY conspiracy. Seattle: Aqueduct Press, 2013.

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universitaẗsbibliothek, 1985.

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universita tsbibliothek, 1985.

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universitätsbibliothek, 1985.

Clark, M. S., and W. J. Wall. Chromosomes. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0073-8.

Milà, Montserrat. Allelic forms of the FMR1 gene: Fragile X syndrome, primary ovarian insufficiency, and tremor ataxia syndrome among others. New York: Nova Science Publishers, Inc., 2015.

Callan, Harold Garnet. Lampbrush chromosomes. Berlin: Springer-Verlag, 1986.

Therman, Eeva. Human Chromosomes. New York, NY: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-0269-8.

Henriques-Gil, N., J. S. Parker, and M. J. Puertas, eds. Chromosomes Today. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-1537-4.

Miller, Orlando J., and Eeva Therman. Human Chromosomes. New York, NY: Springer New York, 2001. http://dx.doi.org/10.1007/978-1-4613-0139-4.

Therman, Eeva, and Millard Susman. Human Chromosomes. New York, NY: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4684-0529-3.

Sumner, A. T., and A. C. Chandley. Chromosomes Today. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1510-0.

Stahl, A., J. M. Luciani, and A. M. Vagner-Capodano, eds. Chromosomes Today. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-010-9166-4.

Callan, Harold Garnet. Lampbrush Chromosomes. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82792-1.

Schmid, Michael, and Indrajit Nanda, eds. Chromosomes Today. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-94-017-1033-6.

Lampbrush chromosomes. Berlin: Springer-Verlag, 1986.

Olmo, Ettore, and Carlo Alberto Redi, eds. Chromosomes Today. Basel: Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8484-6.

Lloyd, J. R. Genesand chromosomes. London: Macmillan, 1986.

Parker, James N., and Philip M. Parker. Triple X syndrome: A bibliography and dictionary for physicians, patients, and genome researchers [to Internet references]. San Diego, CA: ICON Health Publications, 2007.

Wagner, Robert P. Chromosomes: A synthesis. New York: Wiley-Liss, 1993.

McKinlay Gardner, R. J., and David J. Amor. Sex Chromosome Translocations. Edited by R. J. McKinlay Gardner and David J. Amor. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199329007.003.0006.

Kalima, Dara. Two X Chromosomes with an Extra Shot of Melanin. Dara Kalima, 2019.

Project, Human Genome. Chromosome X. Intl Business Pubns USA, 2009.

OPTIZ, JM. Opitz X-Linked Mental Retardation. John Wiley & Sons Inc, 1986.

McKinlay Gardner, R. J., and David J. Amor. Sex Chromosome Aneuploidy and Structural Rearrangement. Edited by R. J. McKinlay Gardner and David J. Amor. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199329007.003.0015.

Brown, Carolyn Janet *. Studies of human X chromosome inactivation. 1991.