Difference between revisions of "Template:Chromosomal abnormalities"
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imported>Nicholas0 m (spacing) |
imported>Naraht (remove redirects) |
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* [[Down syndrome]] | * [[Down syndrome]] | ||
| − | ** [[Chromosome 21 | + | ** [[Chromosome 21|21]] |
* [[Edwards syndrome]] | * [[Edwards syndrome]] | ||
| − | ** [[Chromosome 18 | + | ** [[Chromosome 18|18]] |
* [[Patau syndrome]] | * [[Patau syndrome]] | ||
| − | ** [[Chromosome 13 | + | ** [[Chromosome 13|13]] |
* [[Trisomy 9]] | * [[Trisomy 9]] | ||
* [[Trisomy 8|Warkany syndrome 2]] | * [[Trisomy 8|Warkany syndrome 2]] | ||
| − | ** [[Chromosome 8 | + | ** [[Chromosome 8|8]] |
* [[Cat eye syndrome]]/[[Trisomy 22]] | * [[Cat eye syndrome]]/[[Trisomy 22]] | ||
| − | ** [[Chromosome 22 | + | ** [[Chromosome 22|22]] |
* [[Trisomy 16]] | * [[Trisomy 16]] | ||
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| list2 = | | list2 = | ||
* [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]] | * [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]] | ||
| − | ** [[Chromosome 1 | + | ** [[Chromosome 1|1]] |
* [[Wolf–Hirschhorn syndrome]] | * [[Wolf–Hirschhorn syndrome]] | ||
| − | ** [[Chromosome 4 | + | ** [[Chromosome 4|4]] |
* [[Cri du chat]]/[[Chromosome 5q deletion syndrome]] | * [[Cri du chat]]/[[Chromosome 5q deletion syndrome]] | ||
| − | ** [[Chromosome 5 | + | ** [[Chromosome 5|5]] |
* [[Williams syndrome]] | * [[Williams syndrome]] | ||
| − | ** [[Chromosome 7 | + | ** [[Chromosome 7|7]] |
* [[Jacobsen syndrome]] | * [[Jacobsen syndrome]] | ||
| − | ** [[Chromosome 11 | + | ** [[Chromosome 11|11]] |
* [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]] | * [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]] | ||
| − | ** [[Chromosome 17 | + | ** [[Chromosome 17|17]] |
* [[DiGeorge syndrome]] | * [[DiGeorge syndrome]] | ||
| − | ** [[Chromosome 22 | + | ** [[Chromosome 22|22]] |
* [[22q11.2 distal deletion syndrome]] | * [[22q11.2 distal deletion syndrome]] | ||
| − | ** [[Chromosome 22 | + | ** [[Chromosome 22|22]] |
* [[22q13 deletion syndrome]] | * [[22q13 deletion syndrome]] | ||
| − | ** [[Chromosome 22 | + | ** [[Chromosome 22|22]] |
* ''[[genomic imprinting]]'' | * ''[[genomic imprinting]]'' | ||
| − | ** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15 | + | ** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15|15]]) |
* [[Distal 18q-]]/[[Proximal 18q-]] | * [[Distal 18q-]]/[[Proximal 18q-]] | ||
Revision as of 16:59, 24 January 2020
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