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Older women talking about sex : a discursive analysisJones, Rebecca Loveday January 2003 (has links)
No description available.
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Towards a complete cosmid contig map of the short arm pseudoautosomal regionConway, Daren Joseph January 1997 (has links)
No description available.
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Study of a new family of genes relating to the mammalian testis determining geneCollignon, Jerome Vincent January 1992 (has links)
No description available.
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A prospective study of the dermatoses of pregnancy : correlation of the clinical findings wiht hormonal and immunopathological profilesJones, Samatha Anne Vaughan January 1997 (has links)
No description available.
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Genetic and environmental effects on sex determination in Gammarus duebeni (Crustacea, Amphipoda)Watt, Penelope Jane January 1989 (has links)
No description available.
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236 |
Operationalising performance judgements : sex differences and methods of measurementMiller, Linda January 1991 (has links)
No description available.
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Sexual discourse in the time of AIDSFrankham, Jo January 1994 (has links)
No description available.
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Effects on parental immunization on progeny development in mice and DrosophilaPechan, P. A. January 1987 (has links)
No description available.
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239 |
Gender and age differences in condom use patterns among youth in the Eastern Cape, South Africa: a descriptive and analytical study.Jama, P. Nwabisa January 2006 (has links)
South Africa is estimated to have one of the highest epidemics of HIV infection. Recent youth studies have found that youth aged 15-24 years are increasingly becoming vulnerable to HIV. Condom use is promoted as one of the key HIV prevention methods in South Africa. Face-to-face structured questionnaire interviews were conducted with a volunteer sample of rural active women and men aged 15-26 years living in 70 villages in the Eastern Cape Province. Most of the participants were recruited in schools.
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Sex ratio theory in a splash pool : the sex ratio trait of Tigriopus californicusVoordouw, Maarten Jeroen. 10 April 2008 (has links)
Sex ratio theory makes predictions about how sexually reproducing organisms should allocate their reproductive efforts towards sons and daughters. Fisher predicted that the optimal strategy is one of equal investment (i.e. the 50:50 sex ratio). Subsequent analysis has shown that Fisher's equilibrium sex ratio is contingent on a number of assumptions such as autosomal inheritance of sex ratio alleles, large population size, additive offspring costs, etc. When any of these assumptions are violated the equilibrium sex ratio is not necessarily the one predicted by Fisher. To test sex ratio theory requires systems that exhibit variation for the primary sex ratio. The harpacticoid copepod, Tigriopus californicus is one such system. I have repeatedly detected a large, extra-binomial variance component in the primary sex ratio among full sib families in several natural populations on Vancouver Island. Environmental factors such as temperature and larval density have a mild effect on the primary sex ratio but are not likely to drive sex ratio variation at the population level. Cytoplasmic sex ratio distorters such as Wolbachia are known to cause sex ratio fluctuations in the populations of other crustaceans but were not detected in T. californicus. In the absence of sex-biased mortality, lineage analysis revealed that the sex ratio trait in a local population of T. calijornicus was paternally transmitted. Uniparentally transmitted sex ratio factors are generally under strong selection to increase the proportion of the transmitting sex in their host population. This observation may provide an explanation as to why the population-wide primary sex ratio in T. californicus and other harpacticoid copepods is often male-biased.
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