nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Author index for volume 31
|
|
|
2003 |
31 |
3 |
p. 381-382 2 p. |
artikel |
2 |
Blood group does not correlate with disease severity in patients with Fabry disease (α-galactosidase A deficiency)
|
Linthorst, Gabor E |
|
2003 |
31 |
3 |
p. 324-326 3 p. |
artikel |
3 |
Differential gene expression in the kidney of sickle cell transgenic mice: upregulated genes
|
Rybicki, Anne C |
|
2003 |
31 |
3 |
p. 370-380 11 p. |
artikel |
4 |
Effects of human locus control region elements HS2 and HS3 on human β-globin gene expression in transgenic mouse
|
Jia, Chun-Ping |
|
2003 |
31 |
3 |
p. 360-369 10 p. |
artikel |
5 |
Familial Mediterranean fever with amyloidosis associated with novel exon 2 mutation (S1791) of the MEFV gene
|
Timmann, Christian |
|
2003 |
31 |
3 |
p. 320-323 4 p. |
artikel |
6 |
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans
|
Beutler, Ernest |
|
2003 |
31 |
3 |
p. 305-309 5 p. |
artikel |
7 |
Genotypic and phenotypic heterogeneity of African Americans with primary iron overload
|
Barton, James C |
|
2003 |
31 |
3 |
p. 310-319 10 p. |
artikel |
8 |
Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene☆
|
Gordeuk, Victor R |
|
2003 |
31 |
3 |
p. 299-304 6 p. |
artikel |
9 |
Mutations in GATA1 in both transient myeloproliferative disorder and acute megakaryoblastic leukemia of Down syndrome
|
Greene, Marianne E |
|
2003 |
31 |
3 |
p. 351-356 6 p. |
artikel |
10 |
Possible primary familial and congenital polycythemia locus at 7q22.1-7q22.2
|
Jedlickova, Katerina |
|
2003 |
31 |
3 |
p. 327-331 5 p. |
artikel |
11 |
Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis
|
Sánchez-López, J.Yoaly |
|
2003 |
31 |
3 |
p. 357-359 3 p. |
artikel |
12 |
Regulation of granulocyte and monocyte differentiation by CCAAT/enhancer binding protein α
|
Friedman, Alan D |
|
2003 |
31 |
3 |
p. 338-341 4 p. |
artikel |
13 |
The emerging role of the myeloid Elf-1 like transcription factorin hematopoiesis
|
Lacorazza, H.Daniel |
|
2003 |
31 |
3 |
p. 342-350 9 p. |
artikel |
14 |
Wiskott–Aldrich syndrome in a female with skewed X-chromosome inactivation
|
Andreu, Nuria |
|
2003 |
31 |
3 |
p. 332-337 6 p. |
artikel |