1 – 6 of 6
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2002
-
Mark
ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis
(
- Contribution to journal › Article
-
Mark
Analysis of ten candidate genes in autism by association and linkage
(
- Contribution to journal › Article
- 2001
-
Mark
VATER non-random association of congenital malformations: study based on data from four malformation registers
(
- Contribution to journal › Article
-
Mark
Isolated glycerol kinase deficiency and fanconi anemia [1]
(
- Contribution to journal › Letter
- 2000
-
Mark
OEIS complex--a population study
(
- Contribution to journal › Article
- 1995
-
Mark
Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis
(
- Contribution to journal › Article