| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
|
Shameer, Khader
|
|
2013
|
133 |
1 |
p. 95-109
|
artikel
|
| 2 |
Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome
|
Pastori, Chiara
|
|
2013
|
133 |
1 |
p. 59-67
|
artikel
|
| 3 |
Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography
|
Koran, Mary Ellen I.
|
|
2013
|
133 |
1 |
p. 85-93
|
artikel
|
| 4 |
Genetic testing and genetic counseling among medicaid-enrolled children with autism spectrum disorder in 2001 and 2007
|
Shea, Lindsay
|
|
2013
|
133 |
1 |
p. 111-116
|
artikel
|
| 5 |
Genome-wide association study and meta-analysis of intraocular pressure
|
Ozel, A. Bilge
|
|
2013
|
133 |
1 |
p. 41-57
|
artikel
|
| 6 |
Haptoglobin (HP) and Haptoglobin-related protein (HPR) copy number variation, natural selection, and trypanosomiasis
|
Hardwick, Robert J.
|
|
2013
|
133 |
1 |
p. 69-83
|
artikel
|
| 7 |
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease
|
Warburton, Dorothy
|
|
2013
|
133 |
1 |
p. 11-27
|
artikel
|
| 8 |
The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
|
Stenson, Peter D.
|
|
2013
|
133 |
1 |
p. 1-9
|
artikel
|
| 9 |
The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation
|
Schreml, Julia
|
|
2013
|
133 |
1 |
p. 29-39
|
artikel
|
| 10 |
WNT10A variants are associated with non-syndromic tooth agenesis in the general population
|
Song, Shujuan
|
|
2013
|
133 |
1 |
p. 117-124
|
artikel
|
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