| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A nonimprinted Prader–Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels
|
Stefan, Mihaela
|
|
2005
|
85 |
5 |
p. 630-640
11 p.
|
artikel
|
| 2 |
A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9
|
Boyadjiev, Simeon A.
|
|
2005
|
85 |
5 |
p. 622-629
8 p.
|
artikel
|
| 3 |
Corrigendum to ‘‘Applications of DNA tiling arrays for whole-genome analysis’’ [Genomics 85 (2005) 1–15]
|
Mockler, Todd C.
|
|
2005
|
85 |
5 |
p. 655-
1 p.
|
artikel
|
| 4 |
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes
|
Kamnasaran, Deepak
|
|
2005
|
85 |
5 |
p. 608-621
14 p.
|
artikel
|
| 5 |
Distribution of human β-defensin polymorphisms in various control and cystic fibrosis populations
|
Vankeerberghen, Anne
|
|
2005
|
85 |
5 |
p. 574-581
8 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2005
|
85 |
5 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Erratum to “The mouse Ifi200 gene cluster: Genomic sequence, analysis, and comparison with the human HIN-200 gene cluster” [Genomics 82 (2003) 34–46]
|
Deschamps, Stéphane
|
|
2005
|
85 |
5 |
p. 654-
1 p.
|
artikel
|
| 8 |
Identification of candidate genes in the type 2 diabetes modifier locus using expression QTL
|
Yaguchi, Hiroshi
|
|
2005
|
85 |
5 |
p. 591-599
9 p.
|
artikel
|
| 9 |
Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22
|
Curtiss, Nicole P.
|
|
2005
|
85 |
5 |
p. 600-607
8 p.
|
artikel
|
| 10 |
Linkage disequilibrium analysis identifies an FGFR1 haplotype-tag SNP associated with normal variation in craniofacial shape
|
Coussens, Anna K.
|
|
2005
|
85 |
5 |
p. 563-573
11 p.
|
artikel
|
| 11 |
Mammalian SP/KLF transcription factors: Bring in the family
|
Suske, Guntram
|
|
2005
|
85 |
5 |
p. 551-556
6 p.
|
artikel
|
| 12 |
Molecular characterization of the pericentric inversion of chimpanzee chromosome 11 homologous to human chromosome 9
|
Kehrer-Sawatzki, Hildegard
|
|
2005
|
85 |
5 |
p. 542-550
9 p.
|
artikel
|
| 13 |
Molecular cloning and functional characterization of mouse Nxf family gene products
|
Sasaki, Mitsuho
|
|
2005
|
85 |
5 |
p. 641-653
13 p.
|
artikel
|
| 14 |
Mouse splice mutant generation from ENU-treated ES cells—A gene-driven approach
|
Greber, Boris
|
|
2005
|
85 |
5 |
p. 557-562
6 p.
|
artikel
|
| 15 |
Sense and antisense Foxl2 transcripts in mouse
|
Cocquet, Julie
|
|
2005
|
85 |
5 |
p. 531-541
11 p.
|
artikel
|
| 16 |
The Mass1 frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC
|
Johnson, K.R.
|
|
2005
|
85 |
5 |
p. 582-590
9 p.
|
artikel
|
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