| no |
title |
author |
magazine |
year |
volume |
issue |
page(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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 4 |
European Academy of Andrology (EAA) International Symposium
|
,
|
|
2003
|
112 |
5-6 |
p. 623
|
article
|
| 5 |
Finnish Disease Heritage I:
|
Norio, Reijo
|
|
2003
|
112 |
5-6 |
p. 441-456
|
article
|
| 6 |
Finnish Disease Heritage II: population prehistory and genetic roots of Finns
|
Norio, Reijo
|
|
2003
|
112 |
5-6 |
p. 457-469
|
article
|
| 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
|
article
|
| 8 |
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica
|
Carvajal-Carmona, Luis G.
|
|
2003
|
112 |
5-6 |
p. 534-541
|
article
|
| 9 |
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35
|
Jiao, Xiaodong
|
|
2003
|
112 |
5-6 |
p. 593-599
|
article
|
| 10 |
Genome-wide targeted search for human specific and polymorphic L1 integrations
|
Buzdin, Anton
|
|
2003
|
112 |
5-6 |
p. 527-533
|
article
|
| 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
|
article
|
| 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
|
article
|
| 13 |
No evidence of fetal DNA persistence in maternal plasma after pregnancy
|
Smid, Maddalena
|
|
2003
|
112 |
5-6 |
p. 617-618
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 17 |
The Finnish disease heritage III: the individual diseases
|
Norio, Reijo
|
|
2003
|
112 |
5-6 |
p. 470-526
|
article
|
| 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
|
article
|
Journal description