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A Case Database of Human Ring Chromosome
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[Carrier]a person who has one normal gene and one non-working gene for a recessively inherited disease,or a person with a balanced chromosomal rearrangement. carriers do not usually develop disease but can pass on the non-working copy or an unbalanced chromosome rearrangement to their children.
[Blastomere]the first cells resulting from divisions of a fertilized egg cell
[Blastocyst]a very early stage of embryonic development. about 4-5 days after conception the embryo consists of a circle of cells with fluid in the center and a clump of cells at one end with a thinner layer of cells at the other end.
[Birth defects]an abnormality of structure, function, or body metabolism which often results in a physical or mental handicap. the causemay be genetic or environmental.
[Autosome]any chromosome that is not a sex chromosome. in humans, the autosomes are the numbered chromosomes, numbered from 1 - 22. chromosome 1 is the largest and chromosome 22 is the smallest.
[Angelman syndrome]a conditioncharacterized by severe mental deficiency, developmental delay and growth deficiency and frequent laughter unconnected to emotions of happiness.
[Aneuploidy]the gain or loss of one chromosome compared to the typical chromosome complement, 46.
[Anaphase lag]an error which can occur during cell division where one chromosome simply fails to get incorporated into the nucleus of a daughter cell. the mechanism for trisomic rescue.
[Amniotic sac]the membrane-bound compartment that holds the baby and the amniotic fluid in the uterus.
[Amniotic fluid]the fluid that surrounds the baby, held inside the amniotic sac.


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