nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma
|
Nemesure, Barbara |
|
2003 |
112 |
5-6 |
p. 600-609 |
artikel |
2 |
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics
|
Scott, Clare L. |
|
2003 |
112 |
5-6 |
p. 542-551 |
artikel |
3 |
Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol
|
Lee, Ching Yin |
|
2003 |
112 |
5-6 |
p. 552-562 |
artikel |
4 |
European Academy of Andrology (EAA) International Symposium
|
, |
|
2003 |
112 |
5-6 |
p. 623 |
artikel |
5 |
Finnish Disease Heritage I:
|
Norio, Reijo |
|
2003 |
112 |
5-6 |
p. 441-456 |
artikel |
6 |
Finnish Disease Heritage II: population prehistory and genetic roots of Finns
|
Norio, Reijo |
|
2003 |
112 |
5-6 |
p. 457-469 |
artikel |
7 |
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p
|
Drayna, Dennis |
|
2003 |
112 |
5-6 |
p. 567-572 |
artikel |
8 |
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica
|
Carvajal-Carmona, Luis G. |
|
2003 |
112 |
5-6 |
p. 534-541 |
artikel |
9 |
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35
|
Jiao, Xiaodong |
|
2003 |
112 |
5-6 |
p. 593-599 |
artikel |
10 |
Genome-wide targeted search for human specific and polymorphic L1 integrations
|
Buzdin, Anton |
|
2003 |
112 |
5-6 |
p. 527-533 |
artikel |
11 |
Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome
|
Bénit, Paule |
|
2003 |
112 |
5-6 |
p. 563-566 |
artikel |
12 |
G. Evers-Kiebooms, M.W. Zoeteweij, P.S. Harper (eds): Prenatal testing for late onset neurogenetic diseases
|
Tibben, Aad |
|
2003 |
112 |
5-6 |
p. 621-622 |
artikel |
13 |
No evidence of fetal DNA persistence in maternal plasma after pregnancy
|
Smid, Maddalena |
|
2003 |
112 |
5-6 |
p. 617-618 |
artikel |
14 |
Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia
|
Macpherson, James |
|
2003 |
112 |
5-6 |
p. 619-620 |
artikel |
15 |
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse
|
Peeters, H. |
|
2003 |
112 |
5-6 |
p. 573-580 |
artikel |
16 |
Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approach
|
Pérez-Enciso, Miguel |
|
2003 |
112 |
5-6 |
p. 581-592 |
artikel |
17 |
The Finnish disease heritage III: the individual diseases
|
Norio, Reijo |
|
2003 |
112 |
5-6 |
p. 470-526 |
artikel |
18 |
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels
|
Damcott, Coleen M. |
|
2003 |
112 |
5-6 |
p. 610-616 |
artikel |