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                             39 gevonden resultaten
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
                             39 gevonden resultaten
 
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