| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E
|
Nuinoon, Manit
|
|
2009
|
127 |
3 |
p. 303-314
|
artikel
|
| 2 |
Effects of measured susceptibility genes on cancer risk in family studies
|
Wu, Chih-Chieh
|
|
2009
|
127 |
3 |
p. 349-357
|
artikel
|
| 3 |
Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm
|
LopezJimenez, Nelson
|
|
2009
|
127 |
3 |
p. 325-336
|
artikel
|
| 4 |
Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility
|
Alter, Andrea
|
|
2009
|
127 |
3 |
p. 337-348
|
artikel
|
| 5 |
Genetics of osteoporosis: accelerating pace in gene identification and validation
|
Li, Wen-Feng
|
|
2009
|
127 |
3 |
p. 249-285
|
artikel
|
| 6 |
Jones S, Keynes M (eds): Twelve Galton lectures. A centenary selection with commentaries
|
Harper, Peter S.
|
|
2010
|
127 |
3 |
p. 371-372
|
artikel
|
| 7 |
Large intron 14 rearrangement in APC results in splice defect and attenuated FAP
|
Tuohy, Thérèse M. F.
|
|
2009
|
127 |
3 |
p. 359-369
|
artikel
|
| 8 |
SNPs for a universal individual identification panel
|
Pakstis, Andrew J.
|
|
2009
|
127 |
3 |
p. 315-324
|
artikel
|
| 9 |
The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study
|
Franceschini, Nora
|
|
2009
|
127 |
3 |
p. 295-301
|
artikel
|
| 10 |
The Q223R polymorphism in LEPR is associated with obesity in Pacific Islanders
|
Furusawa, Takuro
|
|
2009
|
127 |
3 |
p. 287-294
|
artikel
|
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