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 |