Difference between revisions of "Template:Chromosomal abnormalities"

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imported>Arcadian
(grouping)
imported>Arcadian
(grouping)
Line 13: Line 13:
  
 
   | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]]
 
   | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]]
   |  list2 = [[Wolf-Hirschhorn syndrome]] (4), [[Cri du chat]] (5), [[Williams syndrome]] (7), [[Angelman syndrome]]/[[Prader-Willi syndrome]] (15), <br>
+
   |  list2 = [[Wolf-Hirschhorn syndrome]] (4), [[Cri du chat]] (5), [[Williams syndrome]] (7), ''[[genomic imprinting]]'' ([[Angelman syndrome]]/[[Prader-Willi syndrome]] (15)), <br>
 
[[Miller-Dieker syndrome]]/[[Smith-Magenis syndrome]] (17), [[22q11.2 deletion syndrome]] (22)
 
[[Miller-Dieker syndrome]]/[[Smith-Magenis syndrome]] (17), [[22q11.2 deletion syndrome]] (22)
  
Line 36: Line 36:
 
|  list4 = [[Philadelphia chromosome]], [[Burkitt's lymphoma]]
 
|  list4 = [[Philadelphia chromosome]], [[Burkitt's lymphoma]]
  
| group5 = Other
+
| group5 = [[Gonadal dysgenesis]]
|  list5 = [[Fragile X syndrome]], [[Gonadal dysgenesis]] ([[Mixed gonadal dysgenesis]]), [[Uniparental disomy]]
+
|  list5 = [[Mixed gonadal dysgenesis]]
 +
 
 +
| group6 = Other
 +
|  list6 = [[Fragile X syndrome]], [[Uniparental disomy]]
 
}}<noinclude>
 
}}<noinclude>
  
 
[[Category:Disease and disorder templates|{{PAGENAME}}]] [[pt:Predefinição:Anomalias cromossômicas]]
 
[[Category:Disease and disorder templates|{{PAGENAME}}]] [[pt:Predefinição:Anomalias cromossômicas]]
 
</noinclude>
 
</noinclude>

Revision as of 22:40, 24 July 2008