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
- 495
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WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victimsKytovuori, L. / Seppanen, A. / Martikainen, M. H. et al. | 2013
- 501
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Serbian high-risk families: extensive results on BRCA mutation spectra and frequencyDobrič / ić / J. et al. | 2013
- 508
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Epithelial–mesenchymal transition-related microRNA-200s regulate molecular targets and pathways in renal cell carcinomaYoshino, H. / Enokida, H. / Itesako, T. et al. | 2013
- 517
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A nonsynonymous variant of IL1A is associated with endometriosis in Japanese populationHata, Y. / Nakaoka, H. / Yoshihara, K. et al. | 2013
- 521
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Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysisKim, J. J. / Park, Y. M. / Yoon, D. et al. | 2013
- 526
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The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitineJaberi, E. / Chitsazian, F. / Ali Shahidi, G. et al. | 2013
- 531
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Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian populationVenkatesh, S. K. / Siddaiah, A. / Padakannaya, P. et al. | 2013
- 539
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Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticityVeerappa, A. M. / Saldanha, M. / Padakannaya, P. et al. | 2013
- 548
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Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot studyInoue, T. / Hattori, K. / Ihara, K. et al. | 2013
- 553
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Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptionsYrigollen, C. M. / Mendoza-Morales, G. / Hagerman, R. et al. | 2013
- 560
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Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in JapanTanaka, K. / Sekijima, Y. / Yoshida, K. et al. | 2013
- 564
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Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophyMatsuura, T. / Kurosaki, T. / Omote, Y. et al. | 2013
- 566
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Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A geneCabral, R. M. / Kurban, M. / Rothman, L. et al. | 2013
- 568
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Further evidence of an association between a genetic variant in BMP7 and treatment response to SSRIs in major depressive disorderEsaki, K. / Kondo, K. / Hatano, M. et al. | 2013