| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genome-wide Association Study Identifies Three Loci Associated with Mean Platelet Volume
|
Meisinger, Christa
|
|
2009
|
84 |
1 |
p. 66-71
6 p.
|
artikel
|
| 2 |
A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan
|
Tompson, Stuart W.
|
|
2009
|
84 |
1 |
p. 72-79
8 p.
|
artikel
|
| 3 |
Association of Genetic Variants at 3q22 with Nephropathy in Patients with Type 1 Diabetes Mellitus
|
He, Bing
|
|
2009
|
84 |
1 |
p. 5-13
9 p.
|
artikel
|
| 4 |
Deleterious Variants of FIG4, a Phosphoinositide Phosphatase, in Patients with ALS
|
Chow, Clement Y.
|
|
2009
|
84 |
1 |
p. 85-88
4 p.
|
artikel
|
| 5 |
Distribution of the Alcohol Dehydrogenase ADH1B∗47His Allele in Eurasia
|
Borinskaya, Svetlana
|
|
2009
|
84 |
1 |
p. 89-92
4 p.
|
artikel
|
| 6 |
Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
|
Chen, Pei-Lung
|
|
2009
|
84 |
1 |
p. 21-34
14 p.
|
artikel
|
| 7 |
Genetic Defects in Surfactant Protein A2 Are Associated with Pulmonary Fibrosis and Lung Cancer
|
Wang, Yongyu
|
|
2009
|
84 |
1 |
p. 52-59
8 p.
|
artikel
|
| 8 |
Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease
|
Beecham, Gary W.
|
|
2009
|
84 |
1 |
p. 35-43
9 p.
|
artikel
|
| 9 |
Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2
|
Neilson, Derek E.
|
|
2009
|
84 |
1 |
p. 44-51
8 p.
|
artikel
|
| 10 |
Low Allele Frequency of ADH1B∗47His in West China and Different ADH1B Haplotypes in Western and Eastern Asia
|
Li, Hui
|
|
2009
|
84 |
1 |
p. 92-94
3 p.
|
artikel
|
| 11 |
Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications
|
Bargal, Ruth
|
|
2009
|
84 |
1 |
p. 80-84
5 p.
|
artikel
|
| 12 |
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
|
Zeharia, Avraham
|
|
2009
|
84 |
1 |
p. 95-
1 p.
|
artikel
|
| 13 |
Mutations of the SYCP3 Gene in Women with Recurrent Pregnancy Loss
|
Bolor, Hasbaira
|
|
2009
|
84 |
1 |
p. 14-20
7 p.
|
artikel
|
| 14 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2009
|
84 |
1 |
p. 3-4
2 p.
|
artikel
|
| 15 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2009
|
84 |
1 |
p. 1-2
2 p.
|
artikel
|
| 16 |
Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels
|
Benyamin, Beben
|
|
2009
|
84 |
1 |
p. 60-65
6 p.
|
artikel
|
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