Chromosome 21: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
Humans have 23 pairs of [[Chromosomes|chromosomes]] (including [[Sex chromosomes|sex chromosomes]]). The twenty first pair of [[Chromosomes|chromosomes is]] described as chromosome 21, this is the smallest human chromosome with 48 million nucleotides and representing 1.5 to 2 percent of the total DNA in cell<ref>http://ghr.nlm.nih.gov/chromosome/21</ref>. During [[DNA replication|DNA replication]], if the [[Spindle fibres|spindle fibres]] fail to separate the chromosomes apart equally, daughter will result in either [[Monosomic|monosomic]] or [[Trisomy|trisomic]]. [[Trisomy 21|Trisomy 21]], a condition in which the [[Karyotype|karyotype]] includes three copies of chromosome 21, is the cause of [[Down Syndrome|Down Syndrome]].<sup></sup> | Humans have 23 pairs of [[Chromosomes|chromosomes]] (including [[Sex chromosomes|sex chromosomes]]). The twenty first pair of [[Chromosomes|chromosomes is]] described as chromosome 21, this is the smallest human chromosome with 48 million nucleotides and representing 1.5 to 2 percent of the total DNA in cell<ref>http://ghr.nlm.nih.gov/chromosome/21</ref>. During [[DNA replication|DNA replication]], if the [[Spindle fibres|spindle fibres]] fail to separate the chromosomes apart equally, daughter will result in either [[Monosomic|monosomic]] or [[Trisomy|trisomic]]. [[Trisomy 21|Trisomy 21]], a condition in which the [[Karyotype|karyotype]] includes three copies of chromosome 21, is the cause of [[Down Syndrome|Down Syndrome]].<sup></sup><br> | ||
Revision as of 16:39, 27 November 2014
Humans have 23 pairs of chromosomes (including sex chromosomes). The twenty first pair of chromosomes is described as chromosome 21, this is the smallest human chromosome with 48 million nucleotides and representing 1.5 to 2 percent of the total DNA in cell[1]. During DNA replication, if the spindle fibres fail to separate the chromosomes apart equally, daughter will result in either monosomic or trisomic. Trisomy 21, a condition in which the karyotype includes three copies of chromosome 21, is the cause of Down Syndrome.