| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Analysis of the coxsackievirus B-adenovirus receptor gene in patients with myocarditis or dilated cardiomyopathy
|
Bowles, Neil E
|
|
2002
|
77 |
3 |
p. 257-259
3 p.
|
artikel
|
| 2 |
Association of the acid phosphatase (ACP1) gene with triglyceride levels in obese women
|
Bottini, Nunzio
|
|
2002
|
77 |
3 |
p. 226-229
4 p.
|
artikel
|
| 3 |
Biochemical defects in eight SRY missense mutations causing XY gonadal dysgenesis
|
Mitchell, Claire L
|
|
2002
|
77 |
3 |
p. 217-225
9 p.
|
artikel
|
| 4 |
Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency
|
Cederbaum, Stephen D
|
|
2002
|
77 |
3 |
p. 195-201
7 p.
|
artikel
|
| 5 |
Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737)
|
Darvish, D
|
|
2002
|
77 |
3 |
p. 252-256
5 p.
|
artikel
|
| 6 |
IFC - Ed. Board
|
|
|
2002
|
77 |
3 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids
|
Ben-Shalom, Efrat
|
|
2002
|
77 |
3 |
p. 202-208
7 p.
|
artikel
|
| 8 |
Metabolism of platelet activating factor by intrapulmonary vascular smooth muscle cells. Effect of oxygen on phospholipase A2 protein expression and activities of acetyl-CoA acetyltransferase and cholinephosphotransferase
|
Ibe, Basil O
|
|
2002
|
77 |
3 |
p. 237-248
12 p.
|
artikel
|
| 9 |
Molecular analysis of PCCB gene in Korean patients with propionic acidemia
|
Kim, Soon Nam
|
|
2002
|
77 |
3 |
p. 209-216
8 p.
|
artikel
|
| 10 |
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
|
Yuen, Yuet-Ping
|
|
2002
|
77 |
3 |
p. 249-251
3 p.
|
artikel
|
| 11 |
Oxygen-induced metabolic changes and transdifferentiation in immature fetal rat lung lipofibroblasts
|
Boros, László G
|
|
2002
|
77 |
3 |
p. 230-236
7 p.
|
artikel
|
| 12 |
Table of Contents
|
|
|
2002
|
77 |
3 |
p. i-
1 p.
|
artikel
|
| 13 |
Two novel genetic lesions and a common BH4-responsive mutation of the PAH gene in Italian patients with hyperphenylalaninemia
|
Bardelli, T
|
|
2002
|
77 |
3 |
p. 260-266
7 p.
|
artikel
|
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