Journal of human genetics
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
Table of contents
- 481
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Genetic determination in onset age of wrist fractureXiong, D. / Wang, W. / Chen, Y. et al. | 2007
- 485
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An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytomaMuscarella, L. A. / Barbano, R. / Augello, B. et al. | 2007
- 492
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Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrumHu, H. / Wu, L. / Feng, Y. et al. | 2007
- 498
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Gap junction coding genes and schizophrenia: a genetic association studyAleksic, B. / Ishihara, R. / Takahashi, N. et al. | 2007
- 502
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Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean womenKim, S. Y. / Lee, J. Y. / Kim, H. Y. et al. | 2007
- 510
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Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseFukuoka, H. / Kanda, Y. / Ohta, S. et al. | 2007
- 516
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The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida riskLinden, I. J. / Heil, S. G. / Heijer, M. et al. | 2007
- 521
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Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS geneBertola, D. b. / Pereira, A. C. / Brasil, A. S. et al. | 2007
- 527
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Polymorphisms of glutathione S-transferase M1, T1 and P1 in patients with reflux esophagitis and Barrett’s esophagusKala, Z. / Dolina, J. / Marek, F. et al. | 2007
- 535
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Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGHCaselli, R. / Speciale, C. / Pescucci, C. et al. | 2007
- 543
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Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathyMatsushita, Y. / Furukawa, T. / Kasanuki, H. et al. | 2007
- 549
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A novel DFNA5 mutation does not cause hearing loss in an Iranian familyLaer, L. / Meyer, N. C. / Malekpour, M. et al. | 2007
- 553
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Mutation identification and characterization of a Taiwanese patient with fucosidosisLin, S. P. / Chang, J. H. / Cadena, M. P. et al. | 2007
- 557
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Failure to confirm association between PDCD1 polymorphisms and rheumatoid arthritis in a Japanese populationIwamoto, T. / Ikari, K. / Inoue, E. et al. | 2007
- 561
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A syndactyly type IV locus maps to 7q36Sato, D. / Liang, D. / Wu, L. et al. | 2007
- 565
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Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestationLiu, J. Y. / Ren, X. / Yang, X. et al. | 2007