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
- 1
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Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placentaMiura, K. / Miyoshi, O. / Yun, K. et al. | 1999
- 10
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Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markersHegele, R. A. / Sun, F. / Harris, S. B. et al. | 1999
- 15
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Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory in the JapaneseMurakami, F. / Shimomura, T. / Kotani, K. et al. | 1999
- 18
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Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancerShin, K.-H. / Ku, J.-L. / Park, J.-G. et al. | 1999
- 22
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Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in JapaneseAkaba, K. / Kimura, T. / Sasaki, A. et al. | 1999
- 26
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Allelic variations of the D2 dopamine receptor gene in children with idiopathic short statureMiyake, H. / Nagashima, K. / Onigata, K. et al. | 1999
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Prevalence of congenital malformations and genetic diseases in KoreaJung, S.-C. / Kim, S.-S. / Yoon, K.-S. et al. | 1999
- 35
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Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missnse mutaitons in mur^0 patientsMikami, H. / Ogasawara, M. / Matsubara, Y. et al. | 1999
- 40
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No latent chromosome damage in oxygen-exposed premature neonatesMehes, K. / Bajnoczky, K. / Adamovich, K. et al. | 1999
- 43
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Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1Hamaguchi, K. / Cong, N. D. / Yanase, T. et al. | 1999
- 48
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Four novel mutaitons of the Fanconi anemia group A gene (FAA) in Japanese patientsNakamura, A. / Matsuura, S. / Tauchi, H. et al. | 1999
- 52
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Molecular cloning, mapping, and characterization of a novel human gene. MTA1-L1, showing homology to a metastasis-associated gene, MTA1Futamura, M. / Nishimori, H. / Shiratsuchi, T. et al. | 1999
- 57
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Localization of human midisatellite and macrosatellite DNA sequences on chromosomes 1 and X in the great apesSamonte, R. V. / Conte, R. A. / Verma, R. S. et al. | 1999
- 60
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Autosomal dominant onychodystrophy and congenital sensorineural deafnessKondoh, T. / Tsuru, A. / Matsumoto, T. et al. | 1999
- 63
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Another observations of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesionsKono, T. / Migita, T. / Koyama, S. et al. | 1999
- 69
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First case of missense mutaiton (LDH-H: R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patientHidaka, K. / Ueda, N. / Hirata, I. et al. | 1999
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Chromosomal mapping of two RBP-J-related genes: Kyo-T and RBP-LTani, S. / Taniwaki, M. / Taniguchi, Y. et al. | 1999
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A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) geneMangino, M. / Torrente, I. / Luca, A. D. et al. | 1999