| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel computational and structural analysis of nsSNPs in CFTR gene
|
George Priya Doss, C.
|
|
2008
|
2 |
1-2 |
p. 23-32
|
artikel
|
| 2 |
A novel computational and structural analysis of nsSNPs in CFTR gene
|
George Priya Doss, C.
|
|
|
2 |
1-2 |
p. 23-32
|
artikel
|
| 3 |
Association of chromosome 9p21 SNPs with cardiovascular phenotypes in morbid obesity using electronic health record data
|
Wood, G. Craig
|
|
2008
|
2 |
1-2 |
p. 33-43
|
artikel
|
| 4 |
Association of chromosome 9p21 SNPs with cardiovascular phenotypes in morbid obesity using electronic health record data
|
Wood, G. Craig
|
|
|
2 |
1-2 |
p. 33-43
|
artikel
|
| 5 |
Genome mirror 2008
|
Kumar, Dhavendra
|
|
2008
|
2 |
1-2 |
p. 51-53
|
artikel
|
| 6 |
Genome mirror 2008
|
Kumar, Dhavendra
|
|
|
2 |
1-2 |
p. 51-53
|
artikel
|
| 7 |
Hippocrates revisited? Old ideals and new realities
|
Lunshof, Jeantine E.
|
|
2008
|
2 |
1-2 |
p. 1-3
|
artikel
|
| 8 |
Hippocrates revisited? Old ideals and new realities
|
Lunshof, Jeantine E.
|
|
|
2 |
1-2 |
p. 1-3
|
artikel
|
| 9 |
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
|
Lee, Ming Ta Michael
|
|
2008
|
2 |
1-2 |
p. 45-49
|
artikel
|
| 10 |
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
|
Lee, Ming Ta Michael
|
|
|
2 |
1-2 |
p. 45-49
|
artikel
|
| 11 |
Molecular genetics of myocardial infarction
|
Yamada, Yoshiji
|
|
2008
|
2 |
1-2 |
p. 7-22
|
artikel
|
| 12 |
Molecular genetics of myocardial infarction
|
Yamada, Yoshiji
|
|
|
2 |
1-2 |
p. 7-22
|
artikel
|
| 13 |
The electronic health record as a primary source of clinical phenotype for genetic epidemiological studies
|
Yamada, Yoshiji
|
|
2008
|
2 |
1-2 |
p. 5
|
artikel
|
| 14 |
The electronic health record as a primary source of clinical phenotype for genetic epidemiological studies
|
Yamada, Yoshiji
|
|
|
2 |
1-2 |
p. 5
|
artikel
|
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