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
- 391
-
Cancer genetics: colorectal cancer as a modelBodmer, W. F. et al. | 2006
- 397
-
Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafishKunkel, L. M. / Bachrach, E. / Bennett, R. R. et al. | 2006
- 407
-
Polymorphisms in the ABO blood group gene in three populations in the New Georgia group of the Solomon IslandsOhashi, J. / Naka, I. / Kimura, R. et al. | 2006
- 412
-
Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluidMiura, S. / Miura, K. / Masuzaki, H. et al. | 2006
- 418
-
COL7A1 mutation G2037E causes epidermal retention of type VII collagenSawamura, D. / Sato-Matsumura, K. / Shibata, S. et al. | 2006
- 424
-
Coexistence of five G6PD variants indicates ethnic complexity of Phuket islanders, Southern ThailandNinokata, A. / Kimura, R. / Samakkarn, U. et al. | 2006
- 429
-
Sequence polymorphisms of the mtDNA control region in a human isolate: the Georgians from SwanetiaAlfonso-Sánchez, M. A. / Martínez-Bouzas, C. / Castro, A. et al. | 2006
- 440
-
Tissue specificity of methylation and expression of human genes coding for neuropeptides and their receptors, and of a human endogenous retrovirus K familyShen, H. m. / Nakamura, A. / Sugimoto, J. et al. | 2006
- 451
-
Complete sequence data support lack of balancing selection on PRNP in a natural Chinese populationZan, Q. / Wen, B. / He, Y. et al. | 2006
- 455
-
A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlationKamada, F. / Kure, S. / Kudo, T. et al. | 2006
- 461
-
A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in NaganoOhata, T. / Yoshida, K. / Sakai, H. et al. | 2006
- 467
-
Genetic encapsulation among Near Eastern populationsShepard, E. M. / Herrera, R. J. et al. | 2006
- 477
-
Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injectionHamanoue, H. / Umezu, N. / Okuda, M. et al. | 2006
- 480
-
Meta-analysis of genome-wide linkage studies for bone mineral densityLee, Y. H. / Rho, Y. H. / Choi, S. J. et al. | 2006
- 487
-
Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindredSpecktor, P. / Cooper, J. G. / Indelman, M. et al. | 2006
- 491
-
Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?Krischek, B. / Narita, A. / Akagawa, H. et al. | 2006
- 495
-
A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiencyKellermayer, R. / Hsu, A. P. / Stankovics, J. z. et al. | 2006
- 498
-
A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontiaTao, R. / Jin, B. / Guo, S. Z. et al. | 2006