Category:Medical genetics task force articles
Pages in category "Medical genetics task force articles"
The following 17 pages are in this category, out of approximately 1,222 total. This list may not reflect recent changes.
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- Talk:1p36 deletion syndrome
- Talk:1q21.1 deletion syndrome
- Talk:1q21.1 duplication syndrome
- Talk:2-Hydroxyglutaric aciduria
- Talk:2-Methylbutyryl-CoA dehydrogenase deficiency
- Talk:2,4 Dienoyl-CoA reductase deficiency
- Talk:2p15-16.1 microdeletion syndrome
- Talk:2q37 deletion syndrome
- Talk:3 hydroxyisobutyric aciduria
- Talk:3-hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Hydroxyisobutyryl-CoA deacylase deficiency
- Talk:3-M syndrome
- Talk:3-Methylcrotonyl-CoA carboxylase deficiency
- Talk:3-Methylglutaconic aciduria
- Talk:3C syndrome
- Talk:3p deletion syndrome