| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genome-wide search for genes predisposing to familial psoriasis by using a stratification approach
|
Samuelsson, L.
|
|
1999
|
105 |
6 |
p. 523-529
|
artikel
|
| 2 |
A genome-wide search for genes predisposing to familial psoriasis by using a stratification approach
|
Samuelsson, L.
|
|
1999
|
105 |
6 |
p. 523-529
|
artikel
|
| 3 |
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp
|
Buiting, K.
|
|
1999
|
105 |
6 |
p. 665-666
|
artikel
|
| 4 |
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp
|
Buiting, K.
|
|
1999
|
105 |
6 |
p. 665-666
|
artikel
|
| 5 |
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3
|
Kiss, H.
|
|
1999
|
105 |
6 |
p. 552-559
|
artikel
|
| 6 |
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3
|
Kiss, H.
|
|
1999
|
105 |
6 |
p. 552-559
|
artikel
|
| 7 |
Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat
|
Denney, R.M.
|
|
1999
|
105 |
6 |
p. 542-551
|
artikel
|
| 8 |
Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat
|
Denney, R.M.
|
|
1999
|
105 |
6 |
p. 542-551
|
artikel
|
| 9 |
BamHI-SacI RFLP and Gm analysis of the immunoglobulin IGHG genes in the Northern Selkups (west Siberia): new haplotypes with deletion, duplication and triplication
|
Osipova, L.P.
|
|
1999
|
105 |
6 |
p. 530-541
|
artikel
|
| 10 |
BamHI-SacI RFLP and Gm analysis of the immunoglobulin IGHG genes in the Northern Selkups (west Siberia): new haplotypes with deletion, duplication and triplication
|
Osipova, L.P.
|
|
1999
|
105 |
6 |
p. 530-541
|
artikel
|
| 11 |
Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism
|
Tachezy, R.
|
|
1999
|
105 |
6 |
p. 564-566
|
artikel
|
| 12 |
Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism
|
Tachezy, R.
|
|
1999
|
105 |
6 |
p. 564-566
|
artikel
|
| 13 |
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8
|
Lüdecke, H.-J.
|
|
1999
|
105 |
6 |
p. 619-628
|
artikel
|
| 14 |
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8
|
Lüdecke, H.-J.
|
|
1999
|
105 |
6 |
p. 619-628
|
artikel
|
| 15 |
Genetic susceptibility to pre-eclampsia and chromosome 7q36
|
Guo, G.
|
|
1999
|
105 |
6 |
p. 641-647
|
artikel
|
| 16 |
Genetic susceptibility to pre-eclampsia and chromosome 7q36
|
Guo, G.
|
|
1999
|
105 |
6 |
p. 641-647
|
artikel
|
| 17 |
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy
|
Bowles, K.R.
|
|
1999
|
105 |
6 |
p. 582-586
|
artikel
|
| 18 |
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy
|
Bowles, K.R.
|
|
1999
|
105 |
6 |
p. 582-586
|
artikel
|
| 19 |
Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age
|
Ketterling, R.P.
|
|
1999
|
105 |
6 |
p. 629-640
|
artikel
|
| 20 |
Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age
|
Ketterling, R.P.
|
|
1999
|
105 |
6 |
p. 629-640
|
artikel
|
| 21 |
High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome
|
Thomas, M.G.
|
|
1999
|
105 |
6 |
p. 577-581
|
artikel
|
| 22 |
High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome
|
Thomas, M.G.
|
|
1999
|
105 |
6 |
p. 577-581
|
artikel
|
| 23 |
Inheritance of heart rate variability: the kibbutzim family study
|
Sinnreich, R.
|
|
1999
|
105 |
6 |
p. 654-661
|
artikel
|
| 24 |
Inheritance of heart rate variability: the kibbutzim family study
|
Sinnreich, R.
|
|
1999
|
105 |
6 |
p. 654-661
|
artikel
|
| 25 |
Letter to human genetics journals
|
Ayme, Segolene
|
|
1999
|
105 |
6 |
p. 667-668
|
artikel
|
| 26 |
MEN I gene mutations in sporadic adrenal adenomas
|
Schulte, K.-M.
|
|
1999
|
105 |
6 |
p. 603-610
|
artikel
|
| 27 |
MEN I gene mutations in sporadic adrenal adenomas
|
Schulte, K.-M.
|
|
1999
|
105 |
6 |
p. 603-610
|
artikel
|
| 28 |
Minisatellite mutational processes reduce Fst estimates
|
Flint, J.
|
|
1999
|
105 |
6 |
p. 567-576
|
artikel
|
| 29 |
Minisatellite mutational processes reduce Fst estimates
|
Flint, J.
|
|
1999
|
105 |
6 |
p. 567-576
|
artikel
|
| 30 |
Molecular analysis of eight mutations in FBN1
|
Halliday, D.
|
|
1999
|
105 |
6 |
p. 587-597
|
artikel
|
| 31 |
Molecular analysis of eight mutations in FBN1
|
Halliday, D.
|
|
1999
|
105 |
6 |
p. 587-597
|
artikel
|
| 32 |
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male
|
Vermeesch, J.R.
|
|
1999
|
105 |
6 |
p. 611-618
|
artikel
|
| 33 |
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male
|
Vermeesch, J.R.
|
|
1999
|
105 |
6 |
p. 611-618
|
artikel
|
| 34 |
Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene
|
Afzal, A.R.
|
|
1999
|
105 |
6 |
p. 648-653
|
artikel
|
| 35 |
Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene
|
Afzal, A.R.
|
|
1999
|
105 |
6 |
p. 648-653
|
artikel
|
| 36 |
Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria
|
Baumer, A.
|
|
1999
|
105 |
6 |
p. 598-602
|
artikel
|
| 37 |
Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria
|
Baumer, A.
|
|
1999
|
105 |
6 |
p. 598-602
|
artikel
|
| 38 |
The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 gene
|
Schmidt, O.
|
|
1999
|
105 |
6 |
p. 662-664
|
artikel
|
| 39 |
The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 gene
|
Schmidt, O.
|
|
1999
|
105 |
6 |
p. 662-664
|
artikel
|
| 40 |
Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency
|
Teraoka, M.
|
|
1999
|
105 |
6 |
p. 560-563
|
artikel
|
| 41 |
Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency
|
Teraoka, M.
|
|
1999
|
105 |
6 |
p. 560-563
|
artikel
|
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