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Journal of Human Genetics|July 2, 2003
Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomaliesErwin Petek, Christian Windpassinger, Burkhard Simma, et al.Journal of Human Genetics|May 17, 2003
Establishment of a method of anonymization of DNA samples in genetic researchKazuo Hara, Kazuhiko Ohe, Takashi Kadowaki, et al.Journal of Human Genetics|July 29, 2003
Genomic structure and alternative splicing of the insulin receptor tyrosine kinase substrate of 53-kDa proteinAtsushi Miyahara, Yuko Okamura-Oho, Toshiyuki Miyashita, et al.Journal of Human Genetics|June 24, 2003
Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testisLi Zeng, Shaohua Gu, Yao Li, et al.Journal of Human Genetics|February 18, 2011
Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in JapanAkiko Abe, Chikahiko Numakura, Kazuki Kijima, et al.Journal of Human Genetics|December 15, 2010
Low prevalence of classical galactosemia in Korean populationBeom Hee Lee, Chong Kun Cheon, Jae-Min Kim, et al.Journal of Human Genetics|January 14, 2011
No association between TNFSF15 and IL23R with ulcerative colitis in KoreansSuk-Kyun Yang, Yusun Jung, Myunghee Hong, et al.Journal of Human Genetics|December 24, 2010
Knowledge gaining by human genetic studies on tuberculosis susceptibilityHui-Qi Qu, Susan P Fisher-Hoch, Joseph B McCormickJournal of Human Genetics|October 8, 2010
Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype associationDana Gabriková, Carina Frykholm, Ulla Friberg, et al.Journal of Human Genetics|December 17, 2010
CASP3 gene single-nucleotide polymorphism (rs72689236) and Kawasaki disease in Taiwanese childrenHo-Chang Kuo, Hong-Ren Yu, Suh-Hang Hank Juo, et al.Pageof 351