nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22
|
Benjes, Suzanne M. |
|
2001 |
109 |
6 |
p. 628-637 |
artikel |
2 |
A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22
|
Benjes, Suzanne M. |
|
2001 |
109 |
6 |
p. 628-637 |
artikel |
3 |
A new strategy for the detection of subtelomeric rearrangements
|
Fauth, Christine |
|
2001 |
109 |
6 |
p. 576-583 |
artikel |
4 |
A new strategy for the detection of subtelomeric rearrangements
|
Fauth, Christine |
|
2001 |
109 |
6 |
p. 576-583 |
artikel |
5 |
Are we hardwired? The role of genes in human behaviour
|
Wilkie, Tom |
|
2001 |
109 |
6 |
p. 682 |
artikel |
6 |
Armenian Y chromosome haplotypes reveal strong regional structure within a single ethno-national group
|
Weale, Michael E. |
|
2001 |
109 |
6 |
p. 659-674 |
artikel |
7 |
Armenian Y chromosome haplotypes reveal strong regional structure within a single ethno-national group
|
Weale, Michael E. |
|
2001 |
109 |
6 |
p. 659-674 |
artikel |
8 |
ASP – a simulation-based power calculator for genetic linkage studies of qualitative traits, using sib-pairs
|
Krawczak, Michael |
|
2001 |
109 |
6 |
p. 675-677 |
artikel |
9 |
ASP – a simulation-based power calculator for genetic linkage studies of qualitative traits, using sib-pairs
|
Krawczak, Michael |
|
2001 |
109 |
6 |
p. 675-677 |
artikel |
10 |
Characterisation of two mutations in the ABCD1 gene leading to low levels of normal ALDP
|
Guimarães, Carla P. |
|
2001 |
109 |
6 |
p. 616-622 |
artikel |
11 |
Characterisation of two mutations in the ABCD1 gene leading to low levels of normal ALDP
|
Guimarães, Carla P. |
|
2001 |
109 |
6 |
p. 616-622 |
artikel |
12 |
Christopher Gillberg and Mary Coleman: The biology of the autistic syndromes, 3rd edn
|
Thapar, Anita |
|
2001 |
109 |
6 |
p. 683 |
artikel |
13 |
Christopher Gillberg and Mary Coleman: The biology of the autistic syndromes, 3rd edn
|
Thapar, Anita |
|
2001 |
109 |
6 |
p. 683 |
artikel |
14 |
Eberhard Passarge: Color Atlas of Genetics. (2nd edition, enlarged and revised)
|
Fleming, Nick |
|
2001 |
109 |
6 |
p. 686 |
artikel |
15 |
Ettore Olmo and Carlo Alberto Redi (eds): Chromosomes today, vol 13
|
Speicher, Michael R. |
|
2001 |
109 |
6 |
p. 685 |
artikel |
16 |
G. Scherer and M. Schmid (eds): Genes and mechanisms in vertebrate sex determination
|
Brockdorff, Neil |
|
2001 |
109 |
6 |
p. 687-688 |
artikel |
17 |
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
|
Kelberman, D. |
|
2001 |
109 |
6 |
p. 638-645 |
artikel |
18 |
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
|
Kelberman, D. |
|
2001 |
109 |
6 |
p. 638-645 |
artikel |
19 |
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
|
Kelberman, D. |
|
|
109 |
6 |
p. 638-645 |
artikel |
20 |
Karen Steinberg: The Genetic Basis of Cancer [CD Rom]
|
France, Elizabeth A. |
|
2001 |
109 |
6 |
p. 681 |
artikel |
21 |
Karen Steinberg: The Genetic Basis of Cancer [CD Rom]
|
France, Elizabeth A. |
|
2001 |
109 |
6 |
p. 681 |
artikel |
22 |
Krystyne E. Wisniewski and Nanbert Zhong (eds): Batten disease: diagnosis, treatment and research. (Advances in Genetics, vol 45)
|
Gardiner, Mark |
|
2001 |
109 |
6 |
p. 684 |
artikel |
23 |
Krystyne E. Wisniewski and Nanbert Zhong (eds): Batten disease: diagnosis, treatment and research. (Advances in Genetics, vol 45)
|
Gardiner, Mark |
|
2001 |
109 |
6 |
p. 684 |
artikel |
24 |
Mutation spectrum and splicing variants in the OPA1 gene
|
Delettre, Cécile |
|
2001 |
109 |
6 |
p. 584-591 |
artikel |
25 |
Mutation spectrum and splicing variants in the OPA1 gene
|
Delettre, Cécile |
|
2001 |
109 |
6 |
p. 584-591 |
artikel |
26 |
Phenotypic variability at the TGF-β1 locus in Camurati-Engelmann disease
|
Campos-Xavier, Ana |
|
2001 |
109 |
6 |
p. 653-658 |
artikel |
27 |
Phenotypic variability at the TGF-β1 locus in Camurati-Engelmann disease
|
Campos-Xavier, Ana |
|
2001 |
109 |
6 |
p. 653-658 |
artikel |
28 |
Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A→G, 2751+2T→A, 296+1G→C, 1717–9T→C-D565G) and one nonsense mutation (E822X) in the CFTR gene
|
Tzetis, Maria |
|
2001 |
109 |
6 |
p. 592-601 |
artikel |
29 |
Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A→G, 2751+2T→A, 296+1G→C, 1717–9T→C-D565G) and one nonsense mutation (E822X) in the CFTR gene
|
Tzetis, Maria |
|
2001 |
109 |
6 |
p. 592-601 |
artikel |
30 |
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease
|
Abraham, Richard |
|
2001 |
109 |
6 |
p. 646-652 |
artikel |
31 |
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease
|
Abraham, Richard |
|
2001 |
109 |
6 |
p. 646-652 |
artikel |
32 |
TGFβ1 allele association with asthma severity
|
Pulleyn, Louise J. |
|
2001 |
109 |
6 |
p. 623-627 |
artikel |
33 |
TGFβ1 allele association with asthma severity
|
Pulleyn, Louise J. |
|
2001 |
109 |
6 |
p. 623-627 |
artikel |
34 |
The HUGO Gene Nomenclature Committee (HGNC)
|
Povey, Sue |
|
2001 |
109 |
6 |
p. 678-680 |
artikel |
35 |
The HUGO Gene Nomenclature Committee (HGNC)
|
Povey, Sue |
|
2001 |
109 |
6 |
p. 678-680 |
artikel |
36 |
The molecular basis of familial hypercholesterolemia in The Netherlands
|
Fouchier, Sigrid W. |
|
2001 |
109 |
6 |
p. 602-615 |
artikel |
37 |
The molecular basis of familial hypercholesterolemia in The Netherlands
|
Fouchier, Sigrid W. |
|
2001 |
109 |
6 |
p. 602-615 |
artikel |
38 |
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family
|
Guipponi, Michel |
|
2001 |
109 |
6 |
p. 569-575 |
artikel |
39 |
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family
|
Guipponi, Michel |
|
2001 |
109 |
6 |
p. 569-575 |
artikel |