Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             15 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group Borck, Guntram
2011
131 2 p. 209-216
artikel
2 Analysis of family- and population-based samples in cohort genome-wide association studies Manichaikul, Ani
2011
131 2 p. 275-287
artikel
3 A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain Williamson, Sarah L.
2011
131 2 p. 187-200
artikel
4 Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children Ouma, Collins
2011
131 2 p. 289-299
artikel
5 Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children Ouma, Collins

131 2 p. 289-299
artikel
6 Meta-analysis of new genome-wide association studies of colorectal cancer risk Peters, Ulrike
2011
131 2 p. 217-234
artikel
7 Michelle Webb (ed): Cancer Susceptibility: Methods and Protocols Alsaegh, Abeer
2011
131 2 p. 315-316
artikel
8 Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH Pineda-Alvarez, Daniel E.
2011
131 2 p. 301-310
artikel
9 Mitochondrial DNA and inflammatory diseases Escames, Germaine
2011
131 2 p. 161-173
artikel
10 Mitochondrial Haplogroup X is associated with successful aging in the Amish Courtenay, Monique D.
2011
131 2 p. 201-208
artikel
11 Preimplantation genetic diagnosis: State of the ART 2011 Harper, Joyce C.
2011
131 2 p. 175-186
artikel
12 Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q Raza, Muhammad Hashim
2011
131 2 p. 311-313
artikel
13 Successful COG8 and PDF overlap is mediated by alterations in splicing and polyadenylation signals Pereira-Castro, Isabel
2011
131 2 p. 265-274
artikel
14 The cell adhesion gene PVRL3 is associated with congenital ocular defects Lachke, Salil A.
2011
131 2 p. 235-250
artikel
15 The impact of Converso Jews on the genomes of modern Latin Americans Velez, C.
2011
131 2 p. 251-263
artikel
                             15 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland