| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions
|
Lachlan, K. L.
|
|
2005
|
118 |
5 |
p. 640-651
|
artikel
|
| 2 |
Admixture-matched case-control study: a practical approach for genetic association studies in admixed populations
|
Tsai, Hui-Ju
|
|
2005
|
118 |
5 |
p. 626-639
|
artikel
|
| 3 |
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3
|
Hassan, Muhammad Jawad
|
|
2005
|
118 |
5 |
p. 605-610
|
artikel
|
| 4 |
Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions
|
Derenko, Miroslava
|
|
2005
|
118 |
5 |
p. 591-604
|
artikel
|
| 5 |
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
|
Hagens, Olivier
|
|
2005
|
118 |
5 |
p. 578-590
|
artikel
|
| 6 |
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation
|
Deprez, Liesbet
|
|
2005
|
118 |
5 |
p. 618-625
|
artikel
|
| 7 |
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3
|
John, Peter
|
|
2005
|
118 |
5 |
p. 665-667
|
artikel
|
| 8 |
Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a ∼0.5-Mb submicroscopic deletion in a patient with mild mental retardation
|
Borg, Katarzyna
|
|
2005
|
118 |
5 |
p. 668
|
artikel
|
| 9 |
Population stratification confounds genetic association studies among Latinos
|
Choudhry, Shweta
|
|
2005
|
118 |
5 |
p. 652-664
|
artikel
|
| 10 |
Ring chromosome 15: characterization by array CGH
|
Glass, Ian A.
|
|
2005
|
118 |
5 |
p. 611-617
|
artikel
|
| 11 |
The neurobeachin gene spans the common fragile site FRA13A
|
Savelyeva, Larissa
|
|
2005
|
118 |
5 |
p. 551-558
|
artikel
|
| 12 |
Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy
|
Shoichet, Sarah A.
|
|
2005
|
118 |
5 |
p. 559-567
|
artikel
|
| 13 |
Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men
|
Hsu, Yi-Hsiang
|
|
2005
|
118 |
5 |
p. 568-577
|
artikel
|
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