| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Bayesian Measure of the Probability of False Discovery in Molecular Genetic Epidemiology Studies
|
Wakefield, Jon
|
|
2008
|
83 |
3 |
p. 424-
1 p.
|
artikel
|
| 2 |
Adaptive Evolution of UGT2B17 Copy-Number Variation
|
Xue, Yali
|
|
2008
|
83 |
3 |
p. 337-346
10 p.
|
artikel
|
| 3 |
A Genome-wide Analysis of Admixture in Uyghurs and a High-Density Admixture Map for Disease-Gene Discovery
|
Xu, Shuhua
|
|
2008
|
83 |
3 |
p. 322-336
15 p.
|
artikel
|
| 4 |
A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
|
Alasti, Fatemeh
|
|
2008
|
83 |
3 |
p. 424-
1 p.
|
artikel
|
| 5 |
A Short History of the American Society of Human Genetics
|
Hirschhorn, Kurt
|
|
2008
|
83 |
3 |
p. 307-310
4 p.
|
artikel
|
| 6 |
Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project
|
Higgins, Anne W.
|
|
2008
|
83 |
3 |
p. 425-427
3 p.
|
artikel
|
| 7 |
C-Terminal Deletions in the ALAS2 Gene Lead to Gain of Function and Cause X-linked Dominant Protoporphyria without Anemia or Iron Overload
|
Whatley, Sharon D.
|
|
2008
|
83 |
3 |
p. 408-414
7 p.
|
artikel
|
| 8 |
DYRK1A-Dosage Imbalance Perturbs NRSF/REST Levels, Deregulating Pluripotency and Embryonic Stem Cell Fate in Down Syndrome
|
Canzonetta, Claudia
|
|
2008
|
83 |
3 |
p. 388-400
13 p.
|
artikel
|
| 9 |
FASTKD2 Nonsense Mutation in an Infantile Mitochondrial Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency
|
Ghezzi, Daniele
|
|
2008
|
83 |
3 |
p. 415-423
9 p.
|
artikel
|
| 10 |
Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment Trait
|
Huyghe, Jeroen R.
|
|
2008
|
83 |
3 |
p. 401-407
7 p.
|
artikel
|
| 11 |
Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
|
Li, Bingshan
|
|
2008
|
83 |
3 |
p. 311-321
11 p.
|
artikel
|
| 12 |
[No title]
|
|
|
2008
|
83 |
3 |
p. 428-429
2 p.
|
artikel
|
| 13 |
Optimized Allotopic Expression of the Human Mitochondrial ND4 Prevents Blindness in a Rat Model of Mitochondrial Dysfunction
|
Ellouze, Sami
|
|
2008
|
83 |
3 |
p. 373-387
15 p.
|
artikel
|
| 14 |
Runs of Homozygosity in European Populations
|
McQuillan, Ruth
|
|
2008
|
83 |
3 |
p. 359-372
14 p.
|
artikel
|
| 15 |
The DNA Wars: Part I
|
Bieber, Frederick R.
|
|
2008
|
83 |
3 |
p. 304-306
3 p.
|
artikel
|
| 16 |
The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research
|
Nelson, Matthew R.
|
|
2008
|
83 |
3 |
p. 347-358
12 p.
|
artikel
|
| 17 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
83 |
3 |
p. 299-300
2 p.
|
artikel
|
| 18 |
This Month in The Journal
|
Williamson, Robin E.
|
|
2008
|
83 |
3 |
p. 297-298
2 p.
|
artikel
|
| 19 |
Victor Almon McKusick, MD, 1921–2008, In Memoriam
|
Valle, David
|
|
2008
|
83 |
3 |
p. 301-303
3 p.
|
artikel
|
Tijdschrift beschrijving