| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Confounding effects of microbiome on the susceptibility of TNFSF15 to Crohn’s disease in the Ryukyu Islands
|
Nakagome, Shigeki
|
|
2017
|
136 |
4 |
p. 387-397
|
artikel
|
| 2 |
Emerging genotype–phenotype relationships in patients with large NF1 deletions
|
Kehrer-Sawatzki, Hildegard
|
|
2017
|
136 |
4 |
p. 349-376
|
artikel
|
| 3 |
Exome analysis of Smith–Magenis-like syndrome cohort identifies de novo likely pathogenic variants
|
Berger, Seth I.
|
|
2017
|
136 |
4 |
p. 409-420
|
artikel
|
| 4 |
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
|
Depienne, Christel
|
|
2017
|
136 |
4 |
p. 463-479
|
artikel
|
| 5 |
Genetic differentiation between upland and lowland populations shapes the Y-chromosomal landscape of West Asia
|
Balanovsky, O.
|
|
2017
|
136 |
4 |
p. 437-450
|
artikel
|
| 6 |
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine
|
Haralambieva, Iana H.
|
|
2017
|
136 |
4 |
p. 421-435
|
artikel
|
| 7 |
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine
|
Haralambieva, Iana H.
|
|
|
136 |
4 |
p. 421-435
|
artikel
|
| 8 |
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
|
Zhang, Jing
|
|
2017
|
136 |
4 |
p. 377-386
|
artikel
|
| 9 |
Integrative multi-omics analysis revealed SNP-lncRNA-mRNA (SLM) networks in human peripheral blood mononuclear cells
|
Xia, Wei
|
|
2017
|
136 |
4 |
p. 451-462
|
artikel
|
| 10 |
Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency
|
Stephen, Joshi
|
|
2017
|
136 |
4 |
p. 399-408
|
artikel
|
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