Difference between revisions of "Talk:Hemochromatosis"
From Bioinformatikpedia
m (Blanked the page) |
|||
| Line 1: | Line 1: | ||
| + | hej u2 :) |
||
| + | nice strukture picture :D |
||
| + | Is there a reason why you summed up some phenotypes under one point in your Phenotype listing? I'm just curious ;) |
||
| + | Did you prefer a unique measure of the iron content (in mg)? otherwise I would change the 3000mg to 3g |
||
| + | The splitting of Pathophysiology into disease mechanism and the "normal" process is good idea. |
||
| + | Wenn I saw your inheritance table, I first wonderd about HFE only occuring for caucasian and then I read further, and hej you described it, nice :) |
||
| + | :D haha MHC class I :D |
||
| + | |||
| + | You really wrote a good wiki entry, I liked reading it :) |
||
Revision as of 21:02, 29 April 2013
hej u2 :) nice strukture picture :D Is there a reason why you summed up some phenotypes under one point in your Phenotype listing? I'm just curious ;) Did you prefer a unique measure of the iron content (in mg)? otherwise I would change the 3000mg to 3g The splitting of Pathophysiology into disease mechanism and the "normal" process is good idea. Wenn I saw your inheritance table, I first wonderd about HFE only occuring for caucasian and then I read further, and hej you described it, nice :)
- D haha MHC class I :D
You really wrote a good wiki entry, I liked reading it :)
