1 – 4 of 4
- show: 15
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
Hematologically important mutations : The autosomal forms of chronic granulomatous disease (third update)
(
- Contribution to journal › Article
-
Mark
Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene
(
- Contribution to journal › Article
- 2007
-
Mark
The variable clinical phenotype of liver glycogen synthase deficiency
(
- Contribution to journal › Article
- 2001
-
Mark
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency
(
- Contribution to journal › Article