| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Defective splicing of Megf7/Lrp4, a regulator of distal limb development, in autosomal recessive mulefoot disease
|
Johnson, Eric B.
|
|
2006
|
88 |
5 |
p. 600-609
10 p.
|
artikel
|
| 2 |
Editorial Board
|
|
|
2006
|
88 |
5 |
p. i-
1 p.
|
artikel
|
| 3 |
GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology
|
Al-Mahdawi, Sahar
|
|
2006
|
88 |
5 |
p. 580-590
11 p.
|
artikel
|
| 4 |
Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18)
|
Towers, Paula R.
|
|
2006
|
88 |
5 |
p. 642-649
8 p.
|
artikel
|
| 5 |
Genomic differences between type strain PG1 and field strains of Mycoplasma mycoides subsp. mycoides small-colony type
|
Bischof, Daniela F.
|
|
2006
|
88 |
5 |
p. 633-641
9 p.
|
artikel
|
| 6 |
Identical mutation in a novel retinal gene causes progressive rod–cone degeneration in dogs and retinitis pigmentosa in humans
|
Zangerl, Barbara
|
|
2006
|
88 |
5 |
p. 551-563
13 p.
|
artikel
|
| 7 |
Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle
|
Duchesne, A.
|
|
2006
|
88 |
5 |
p. 610-621
12 p.
|
artikel
|
| 8 |
Identification of a newly spliced exon in the mouse Ilf3 gene generating two long and short isoforms of Ilf3 and NF90
|
Viranaicken, Wildriss
|
|
2006
|
88 |
5 |
p. 622-632
11 p.
|
artikel
|
| 9 |
In silico identification and Bayesian phylogenetic analysis of multiple new mammalian kallikrein gene families
|
Elliott, Marc B.
|
|
2006
|
88 |
5 |
p. 591-599
9 p.
|
artikel
|
| 10 |
Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod–cone degeneration interval and identifies ancestral disease-transmitting chromosome
|
Goldstein, Orly
|
|
2006
|
88 |
5 |
p. 541-550
10 p.
|
artikel
|
| 11 |
Molecular characterization of the porcine surfactant, pulmonary-associated protein C gene
|
Cirera, S.
|
|
2006
|
88 |
5 |
p. 659-668
10 p.
|
artikel
|
| 12 |
Monomorphism of human cytochrome c
|
Bertini, Ivano
|
|
2006
|
88 |
5 |
p. 669-672
4 p.
|
artikel
|
| 13 |
Mutational spectrum in the recent human genome inferred by single nucleotide polymorphisms
|
Jiang, Cizhong
|
|
2006
|
88 |
5 |
p. 527-534
8 p.
|
artikel
|
| 14 |
SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population
|
Kim, Kwang Joong
|
|
2006
|
88 |
5 |
p. 535-540
6 p.
|
artikel
|
| 15 |
The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution
|
Bodega, B.
|
|
2006
|
88 |
5 |
p. 564-571
8 p.
|
artikel
|
| 16 |
The human HYMAI/PLAGL1 differentially methylated region acts as an imprint control region in mice
|
Arima, Takahiro
|
|
2006
|
88 |
5 |
p. 650-658
9 p.
|
artikel
|
| 17 |
The implications of DNA transposons in the evolution of P elements in zebrafish (Danio rerio)
|
Hagemann, Sylvia
|
|
2006
|
88 |
5 |
p. 572-579
8 p.
|
artikel
|
| 18 |
Unexpected biochemical and pharmacogenetic consequences of SNPs and haplotypes: a cautionary tale for human molecular genetics and epidemiology
|
Reichardt, Juergen K.V.
|
|
2006
|
88 |
5 |
p. 673-674
2 p.
|
artikel
|
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