Results
|
21.
|
|
|
22.
|
|
|
23.
|
|
|
24.
|
|
|
25.
|
Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families. [electronic resource] by
- Kleijer, W J
- Garritsen, V H
- Linnebank, M
- Mooyer, P
- Huijmans, J G M
- Mustonen, A
- Simola, K O J
- Arslan-Kirchner, M
- Battini, R
- Briones, P
- Cardo, E
- Mandel, H
- Tschiedel, E
- Wanders, R J A
- Koch, H G
Producer: 20030325
In:
Journal of inherited metabolic disease vol. 25
Availability: No items available.
|
|
26.
|
|
|
27.
|
Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS. [electronic resource] by
- Aebi, M
- Helenius, A
- Schenk, B
- Barone, R
- Fiumara, A
- Berger, E G
- Hennet, T
- Imbach, T
- Stutz, A
- Bjursell, C
- Uller, A
- Wahlström, J G
- Briones, P
- Cardo, E
- Clayton, P
- Winchester, B
- Cormier-Dalre, V
- de Lonlay, P
- Cuer, M
- Dupré, T
- Seta, N
- de Koning, T
- Dorland, L
- de Loos, F
- Kupers, L
Producer: 20001031
In:
Glycoconjugate journal vol. 16
Availability: No items available.
|