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
- 357
-
Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell linesAriyama, Y. / Mori, T. / Shinomiya, T. et al. | 1999
- 364
-
A novel LDLR mutation, H190Y, in a Utah kindred with familial HypercholesterolemiaHopkins, P. N. / Wu, L. L. / Stephenson, S. H. et al. | 1999
- 368
-
Mutation screening of phenylketonuria in the Far East of RussiaSueoka, H. / Moshinetsky, A. / Nagao, M. et al. | 1999
- 372
-
Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitisNatori, K. / Tamari, M. / Watanabe, O. et al. | 1999
- 377
-
Molecular characterization of galactokinase deficiency in Japanese patientsAsada, M. / Okano, Y. / Imamura, T. et al. | 1999
- 383
-
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainBhalla, K. / Eyre, H. J. / Whitmore, S. A. et al. | 1999
- 388
-
Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicityScrimshaw, B. J. / Faed, J. M. / Tate, W. P. et al. | 1999
- 391
-
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complexZhang, H. / Nanba, E. / Yamamoto, T. et al. | 1999
- 397
-
Cloning and characterization of the human UDP-N-acetylglucosamine: -1,3-D-mannoside -1,4-N-acetylglucosaminyltransferase IV-homologue (hGnT-IV-H) geneFurukawa, T. / Youssef, E. M. / Yatsuoka, T. et al. | 1999
- 402
-
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) geneNakajima, T. / Hamakubo, T. / Kodama, T. et al. | 1999
- 408
-
The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dinucleotide repeat at the hCAD locusSugimoto, N. / Fukuda, Y. / Saito-Ohara, F. et al. | 1999
- 412
-
Prader-Willi syndrome in a child with XYYHonma, A. / Ishii, R. / Ito, A. et al. | 1999
- 414
-
A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locusMorishima, K. / Matsuura, S. / Tauchi, H. et al. | 1999
- 416
-
Novel polymorphisms in the upstream region of the human dopamine D4 receptor (DRD4) geneMitsuyasu, H. / Ozawa, H. / Takeda, Y. et al. | 1999
- 419
-
CA repeat polymorphism in the promoter region of the COL1A2 geneDietzsch, E. / Parker, M. I. et al. | 1999
- 421
-
A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) geneIwaki, K. / Nakajima, T. / Ota, N. et al. | 1999
- 423
-
An Ile/Val polymorphism at codon 1464 of the A TP7A geneOgawa, A. / Yamamoto, S. / Takayanagi, M. et al. | 1999
- 425
-
Dinucleotide repeat polymorphism in the third intron of the NRAMP2/DMT1 geneKishi, F. / Fujishima, S. / Tabuchi, M. et al. | 1999
- 428
-
Novel variants in the promoter region of the CREB gene in schizophrenic patientsKawanishi, Y. / Harada, S. / Tachikawa, H. et al. | 1999