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Journal of Human Genetics|September 30, 2026
MC1R variants in four Chinese children with red hair and hypopigmentationYingzi Zhang, Qiaorong Huang, Xiaojing Chen, et al.Journal of Human Genetics|November 4, 2026
Clinical genetics and genetic counseling in the era of disease-modifying therapies for dementia: lessons from JapanKatsuya Nakamura, Yoshiki SekijimaJournal of Human Genetics|August 15, 2001
Cloning and sequencing of a novel human gene that encodes a putative target protein of Nesh-SH3S Matsuda, C Iriyama, S Yokozaki, et al.Journal of Human Genetics|August 15, 2001
Single nucleotide polymorphisms of the fukutin geneH Cao, J Yuen, R A HegeleJournal of Human Genetics|August 15, 2001
Single nucleotide polymorphisms of the very low density lipoprotein receptor (VLDLR) geneS E Near, J Wang, R A HegeleJournal of Human Genetics|October 6, 2001
Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) geneR Ishida, Y Ezura, H Iwasaki, et al.Journal of Human Genetics|October 6, 2001
Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysisN Shiroma, N Kanazawa, M Izumi, et al.Journal of Human Genetics|October 6, 2001
Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinicsH Nagata, K Kumahara, T Tomemori, et al.Journal of Human Genetics|April 6, 2001
Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire geneM Kajita, H Iwasaki, N Ota, et al.Journal of Human Genetics|April 6, 2001
Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire geneY Shinohara, H Iwasaki, N Ota, et al.Pageof 353