| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alterations in CDH15 and KIRREL3 in Patients with Mild to Severe Intellectual Disability
|
Bhalla, Kavita
|
|
2008
|
83 |
6 |
p. 703-713
11 p.
|
artikel
|
| 2 |
A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)
|
Lin, Pengfei
|
|
2008
|
83 |
6 |
p. 752-759
8 p.
|
artikel
|
| 3 |
Association Mapping and Significance Estimation via the Coalescent
|
Kimmel, Gad
|
|
2008
|
83 |
6 |
p. 675-683
9 p.
|
artikel
|
| 4 |
Divergence between Human Populations Estimated from Linkage Disequilibrium
|
Sved, John A.
|
|
2008
|
83 |
6 |
p. 737-743
7 p.
|
artikel
|
| 5 |
Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis
|
Yang, Tie-Lin
|
|
2008
|
83 |
6 |
p. 663-674
12 p.
|
artikel
|
| 6 |
Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation
|
Ji, Yanli
|
|
2008
|
83 |
6 |
p. 760-768
9 p.
|
artikel
|
| 7 |
Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy
|
Compton, Alison G.
|
|
2008
|
83 |
6 |
p. 714-724
11 p.
|
artikel
|
| 8 |
Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
|
Alazami, Anas M.
|
|
2008
|
83 |
6 |
p. 684-691
8 p.
|
artikel
|
| 9 |
Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
|
Matsuo, Hirotaka
|
|
2008
|
83 |
6 |
p. 795-
1 p.
|
artikel
|
| 10 |
Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
|
Matsuo, Hirotaka
|
|
2008
|
83 |
6 |
p. 744-751
8 p.
|
artikel
|
| 11 |
No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50
|
Hunter, Jessica Ezzell
|
|
2008
|
83 |
6 |
p. 692-702
11 p.
|
artikel
|
| 12 |
PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption
|
Decker, Eva
|
|
2008
|
83 |
6 |
p. 781-786
6 p.
|
artikel
|
| 13 |
Ribosomal Protein L5 and L11 Mutations Are Associated with Cleft Palate and Abnormal Thumbs in Diamond-Blackfan Anemia Patients
|
Gazda, Hanna T.
|
|
2008
|
83 |
6 |
p. 769-780
12 p.
|
artikel
|
| 14 |
The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula
|
Adams, Susan M.
|
|
2008
|
83 |
6 |
p. 725-736
12 p.
|
artikel
|
| 15 |
The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population
|
Jakkula, Eveliina
|
|
2008
|
83 |
6 |
p. 787-794
8 p.
|
artikel
|
| 16 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
83 |
6 |
p. 661-662
2 p.
|
artikel
|
| 17 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2008
|
83 |
6 |
p. 659-660
2 p.
|
artikel
|
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