| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Closing the Gap: Inverting the Genetics Curriculum to Ensure an Informed Public
|
Dougherty, Michael J.
|
|
2009
|
85 |
1 |
p. 6-12
7 p.
|
artikel
|
| 2 |
Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies
|
Lefeber, Dirk J.
|
|
2009
|
85 |
1 |
p. 76-86
11 p.
|
artikel
|
| 3 |
Diverse Evolutionary Histories for β-adrenoreceptor Genes in Humans
|
Cagliani, Rachele
|
|
2009
|
85 |
1 |
p. 64-75
12 p.
|
artikel
|
| 4 |
Gene Conversion between the X Chromosome and the Male-Specific Region of the Y Chromosome at a Translocation Hotspot
|
Rosser, Zoë H.
|
|
2009
|
85 |
1 |
p. 130-134
5 p.
|
artikel
|
| 5 |
Gene Ontology Analysis of GWA Study Data Sets Provides Insights into the Biology of Bipolar Disorder
|
Holmans, Peter
|
|
2009
|
85 |
1 |
p. 13-24
12 p.
|
artikel
|
| 6 |
Genome-wide Study of Families with Absolute Pitch Reveals Linkage to 8q24.21 and Locus Heterogeneity
|
Theusch, Elizabeth
|
|
2009
|
85 |
1 |
p. 112-119
8 p.
|
artikel
|
| 7 |
Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations
|
Boissel, Sarah
|
|
2009
|
85 |
1 |
p. 106-111
6 p.
|
artikel
|
| 8 |
Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene
|
Wu, Xiao-lin
|
|
2009
|
85 |
1 |
p. 53-63
11 p.
|
artikel
|
| 9 |
Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2
|
Guernsey, Duane L.
|
|
2009
|
85 |
1 |
p. 120-129
10 p.
|
artikel
|
| 10 |
Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy
|
Verkerk, Annemieke J.M.H.
|
|
2009
|
85 |
1 |
p. 40-52
13 p.
|
artikel
|
| 11 |
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39
|
Schultz, Julie M.
|
|
2009
|
85 |
1 |
p. 25-39
15 p.
|
artikel
|
| 12 |
PRKCA: A Positional Candidate Gene for Body Mass Index and Asthma
|
Murphy, Amy
|
|
2009
|
85 |
1 |
p. 87-96
10 p.
|
artikel
|
| 13 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2009
|
85 |
1 |
p. 3-5
3 p.
|
artikel
|
| 14 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2009
|
85 |
1 |
p. 1-2
2 p.
|
artikel
|
| 15 |
WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
|
Bohring, Axel
|
|
2009
|
85 |
1 |
p. 97-105
9 p.
|
artikel
|
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