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In humans, the sex of a person is controlled by genes found on sex chromosomes.
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There are two SCs: Long one X and short one Y.
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Women = XX, Men = YY.
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The other 44 chromosomes are autosomes.
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During meiosis, the sex chromosomes seperate therefore eggs can only have Xs and sperm can have X or Y.
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Hence, sperm dictate what sex a child will be.
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Not all genes on SCs are involved in development of sexuality. Many have nothing to do with sex at all.
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These genes are sex-linked genes.
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Sex-linked gene's inhertiance does not follow normal monohybrid crosses cos of the lack of genes on Y-chrom.
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Males =\= heterozygous for such sex-linked genes.
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Instead, they always express these genes in their phenotype regardless of dominance or recessivness.
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Two e.g.s are the ges for colour vision and blood clotting factor (called factor 8 but you don't need to know this).
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The mutant recessive alleles give colour blindness and haemophilia.
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A good example of haemophilia and genetics is the royal family.
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Therefore, a colour-blind woman, having children to a normal man, will have boys who are colour-blind and girls who, although carriers of the gene, have normal colour vision.
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