Chang E., Harley C. B. 1995. Telomere length and replicative aging in human vascular tissues.
138
Austad S. 1997.
139
Slagboom P. E., Droog S., Boomsma D. I. 1994. Genetic determination of telomere size in humans: a twin study of three age groups.
140
Ivanova R. et al. 1998. HLA-DR alleles display sex-dependent effects on survival and discriminate between individual and familiar longevity.
141
Austad S. 1997.
142
Feng J. et al. 1995. The RNA component of human telomerase.
143
Holm V. et al. 1993. Prader-Willi syndrome: consensus diagnostic criteria.
144
Angelman H. 1965. ‘Puppet’ children.
145
McGrath J., Solter D. 1984. Completion of mouse embryogenesis requires both the maternal and paternal genomes.
Barton S. C., Surami M. A. H., Norris M. L. 1984. Role of paternal and maternal genomes in mouse development.
146
Haig D., Westoby M. 1989. Parent-specific gene expression and the triploid endosperm.
147
Haig D., Graham C. 1991. Genomic imprinting and the strange case of the insulin-like growth factor II receptor.
148
Dawson W. 1965. Fertility and size inheritance in a Peromyscus species cross.
Mestel R. 1998. The genetic battle of the sexes.
149
Hurst L. D., McVean G. T. 1997. Growth effects of uniparental disomies and the conflict theory of genomic imprinting.
Hurst L. D. 1997. Evolutionary theories of genomic imprinting. In: Reik W., Surani A. (eds),
150
Horsthemke B. 1997. Imprinting in the Prader-Willi/Angelman syndrome region on human chromosome 15. In: Reik W., Surani A. (eds),