Turner sydrome: Difference between revisions
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Turner Sydrome is a monosomy of the X [[Chromosome|chromosome]] resulting in the karyotype 45, X. Females are the sex affected | Turner Sydrome is a monosomy of the X [[Chromosome|chromosome]] which is lacking of one X chromosome resulting in the karyotype 45, X. Females are the sex affected. Although they have female [[Phenotype|phenotypic]] characteristics, they are short and do not reach sexual maturity. <ref name="null">Hartl D., and Jones E,(2009):Analysis of Genes and Genomes: page 269</ref> | ||
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'''<u>References</u>''' | '''<u>References</u>''' | ||
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Revision as of 18:37, 11 November 2012
Turner Sydrome is a monosomy of the X chromosome which is lacking of one X chromosome resulting in the karyotype 45, X. Females are the sex affected. Although they have female phenotypic characteristics, they are short and do not reach sexual maturity. [1]
References
- ↑ Hartl D., and Jones E,(2009):Analysis of Genes and Genomes: page 269