Journal of human genetics
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Table of contents
- 285
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Expression and phylogenetic analyses of human endogenous retrovirus HC2 belonging to the HERV-T family in human tissues and cancer cellsYi, J. M. / Kim, H. S. et al. | 2007
- 297
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Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoterMaina, E. N. / Webb, T. / Soni, S. et al. | 2007
- 308
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Population history of the Dniester–Carpathians: evidence from Alu markersVarzari, A. / Stephan, W. / Stepanov, V. et al. | 2007
- 317
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Polymorphic Alu insertions and the genetic structure of Iberian BasquesGarcía-Obregón, S. / Alfonso-Sánchez, M. A. / Pérez-Miranda, A. M. et al. | 2007
- 328
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Glucocorticoid-induced granzyme A expression can be used as a marker of glucocorticoid sensitivity for acute lymphoblastic leukemia therapyMyoumoto, A. / Nakatani, K. / Koshimizu, T. a. et al. | 2007
- 334
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Paroxysmal kinesigenic choreoathetosis (PKC): confirmation of linkage to 16p11-q21, but unsuccessful detection of mutations among 157 genes at the PKC-critical region in seven PKC familiesKikuchi, T. / Nomura, M. / Tomita, H. et al. | 2007
- 342
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Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphismsZahorakova, D. / Rosipal, R. / Hadac, J. et al. | 2007
- 349
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Molecular and clinical analyses of Japanese patients with carbamoylphosphate synthetase 1 (CPS1) deficiencyKurokawa, K. / Yorifuji, T. / Kawai, M. et al. | 2007
- 355
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Identification of polymorphisms in human interleukin-27 and their association with asthma in a Korean populationChae, S. C. / Li, C. S. / Kim, K. M. et al. | 2007
- 362
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The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cellsYoshida, T. / Tomozawa, Y. / Arisato, T. et al. | 2007
- 370
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A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype–genotype correlationKondoh, T. / Okamoto, N. / Norimatsu, N. et al. | 2007
- 374
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Systematic assessment of the tagging polymorphisms of the COL1A1 gene for high myopiaLiang, C. L. / Hung, K. S. / Tsai, Y. Y. et al. | 2007
- 378
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Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levelsSharma, M. / Mehla, K. / Batra, J. et al. | 2007
- 384
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Assessment of the contribution of the LOC387715 gene polymorphism in a family with exudative age-related macular degeneration and heterozygous CFH variant (Y402H)Shastry, B. S. et al. | 2007
- 388
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The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South AmericaUrreizti, R. / Asteggiano, C. / Bermudez, M. et al. | 2007