| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Association of HLA class I with severe acute respiratory syndrome coronavirus infection
|
Lin, Marie
|
|
2003
|
4 |
1 |
|
artikel
|
| 2 |
Effect of human leukocyte antigen heterozygosity on infectious disease outcome: The need for allele-specific measures
|
Lipsitch, Marc
|
|
2003
|
4 |
1 |
|
artikel
|
| 3 |
Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish men with prostate cancer
|
Hamel, Nancy
|
|
2003
|
4 |
1 |
|
artikel
|
| 4 |
Frequency of CHEK2*1100delC in New York breast cancer cases and controls
|
Offit, Kenneth
|
|
2003
|
4 |
1 |
|
artikel
|
| 5 |
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen
|
Adams, Gaye T
|
|
2003
|
4 |
1 |
|
artikel
|
| 6 |
Genetic study of common variants at the Apo E, Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD
|
Baroni, Marco G
|
|
2003
|
4 |
1 |
|
artikel
|
| 7 |
HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central Alabama
|
Barton, James C
|
|
2003
|
4 |
1 |
|
artikel
|
| 8 |
Lamin A/C truncation in dilated cardiomyopathy with conduction disease
|
MacLeod, Heather M
|
|
2003
|
4 |
1 |
|
artikel
|
| 9 |
Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome
|
Selvaraju, Veeriah
|
|
2003
|
4 |
1 |
|
artikel
|
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