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41 results found

no	title	author	magazine	year	volume	issue	page(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	article
2	A genome-wide search for genes predisposing to familial psoriasis by using a stratification approach	Samuelsson, L.		1999	105	6	p. 523-529	article
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	article
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	article
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	article
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	article
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	article
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	article
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	article
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	article
11	Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism	Tachezy, R.		1999	105	6	p. 564-566	article
12	Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism	Tachezy, R.		1999	105	6	p. 564-566	article
13	Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8	Lüdecke, H.-J.		1999	105	6	p. 619-628	article
14	Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8	Lüdecke, H.-J.		1999	105	6	p. 619-628	article
15	Genetic susceptibility to pre-eclampsia and chromosome 7q36	Guo, G.		1999	105	6	p. 641-647	article
16	Genetic susceptibility to pre-eclampsia and chromosome 7q36	Guo, G.		1999	105	6	p. 641-647	article
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	article
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	article
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	article
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	article
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	article
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	article
23	Inheritance of heart rate variability: the kibbutzim family study	Sinnreich, R.		1999	105	6	p. 654-661	article
24	Inheritance of heart rate variability: the kibbutzim family study	Sinnreich, R.		1999	105	6	p. 654-661	article
25	Letter to human genetics journals	Ayme, Segolene		1999	105	6	p. 667-668	article
26	MEN I gene mutations in sporadic adrenal adenomas	Schulte, K.-M.		1999	105	6	p. 603-610	article
27	MEN I gene mutations in sporadic adrenal adenomas	Schulte, K.-M.		1999	105	6	p. 603-610	article
28	Minisatellite mutational processes reduce Fst estimates	Flint, J.		1999	105	6	p. 567-576	article
29	Minisatellite mutational processes reduce Fst estimates	Flint, J.		1999	105	6	p. 567-576	article
30	Molecular analysis of eight mutations in FBN1	Halliday, D.		1999	105	6	p. 587-597	article
31	Molecular analysis of eight mutations in FBN1	Halliday, D.		1999	105	6	p. 587-597	article
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	article
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	article
34	Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene	Afzal, A.R.		1999	105	6	p. 648-653	article
35	Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene	Afzal, A.R.		1999	105	6	p. 648-653	article
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	article
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	article
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	article
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	article
40	Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency	Teraoka, M.		1999	105	6	p. 560-563	article
41	Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency	Teraoka, M.		1999	105	6	p. 560-563	article

41 results found

Koninklijke Bibliotheek - National Library of the Netherlands