| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3
|
Mendoza, Gustavo
|
|
2006
|
120 |
5 |
p. 653-662
|
artikel
|
| 2 |
A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient
|
Tran, Van Khanh
|
|
2006
|
120 |
5 |
p. 737-742
|
artikel
|
| 3 |
Association of Hck genetic polymorphisms with gene expression and COPD
|
Zhang, Xiaozhu
|
|
2006
|
120 |
5 |
p. 681-690
|
artikel
|
| 4 |
Elevated male European and female African contributions to the genomes of African American individuals
|
Lind, Joanne M.
|
|
2006
|
120 |
5 |
p. 713-722
|
artikel
|
| 5 |
Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury
|
Fornage, Myriam
|
|
2006
|
120 |
5 |
p. 671-680
|
artikel
|
| 6 |
Fibrillin I gene polymorphism is associated with tall stature of normal individuals
|
Mamada, Mitsukazu
|
|
2006
|
120 |
5 |
p. 733-735
|
artikel
|
| 7 |
Genetics of preeclampsia: paradigm shifts
|
Oudejans, Cees B. M.
|
|
2006
|
120 |
5 |
p. 607-612
|
artikel
|
| 8 |
High-resolution mapping of DNA methylation in human genome using oligonucleotide tiling array
|
Hayashi, Hiroshi
|
|
2006
|
120 |
5 |
p. 701-711
|
artikel
|
| 9 |
Ian D. Young: Medical genetics
|
Leonard, Samantha
|
|
2006
|
120 |
5 |
p. 747
|
artikel
|
| 10 |
Identifying genes underlying skin pigmentation differences among human populations
|
Myles, Sean
|
|
2006
|
120 |
5 |
p. 613-621
|
artikel
|
| 11 |
Lack of association between rs7566605 and obesity in a Chinese population
|
Feng, Yan
|
|
2006
|
120 |
5 |
p. 743-745
|
artikel
|
| 12 |
Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans
|
Xing, Chao
|
|
2006
|
120 |
5 |
p. 623-631
|
artikel
|
| 13 |
Paul Polani and the development of medical genetics
|
Harper, Peter S.
|
|
2006
|
120 |
5 |
p. 723-731
|
artikel
|
| 14 |
Predictors of uptake of obesity genetic testing among affected adults
|
Segal, Mary E.
|
|
2006
|
120 |
5 |
p. 641-652
|
artikel
|
| 15 |
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients
|
Tompson, Stuart W. J.
|
|
2006
|
120 |
5 |
p. 663-670
|
artikel
|
| 16 |
Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica
|
Celedón, Juan C.
|
|
2006
|
120 |
5 |
p. 691-699
|
artikel
|
| 17 |
The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model
|
Clark, Rhonda M.
|
|
2006
|
120 |
5 |
p. 633-640
|
artikel
|
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