Biomedical subjects
Publications and source records attributed to S R Wilson.
Renal pseudotumors--both intrinsic and extrinsic--are numerous. On a recent urogram, performed with abdominal pressure and tomography, a mass lesion was simulated by the gas-filled colon. The problem was resolved with a combination of ultrasonography, nephrotomography, and barium enema examinations.
Current therapy for metastatic non-seminomatous testis tumors is effective but toxic. Careful investigation is needed to select those who need treatment and yet avoid needless toxicity in patients who have no disease. Current radiographic investigations and measurement of two biochemical tumor markers (AFP & BHCG) provided accurate monitoring in 19 patients. Preoperative urography and lymphography correctly predicted the presence or absence of retroperitoneal metastases in 9 of 12 patients but did not show microsocpic metastases in 3. There was good correlation between the clinical, readiographic and biochemical evidence of disease progression and regression. Serial ultrasonography and tumor marker determinations were particularly useful in following asymptomatic abdominal metastases. Radiography and tumor marker determinations each have specific advantages which make them complementary.
For the determination of the mode of inheritance of a disease or disorder familial data is often used and is usually presented in frequency form. This data has usually been obtained from a single set of nuclear families and so the estimates of the frequencies in relatives of those affected are not independent of one another and this makes inference concerning the mode of inheritance difficult. The exact degree of the correlation between estimates is not easy to determine. In this paper expressions are derived for the asymptotic variances of estimates and for the covariances and correlations between the basic pairs of intrafamilial frequency estimates for families of a given structure, and the extension to families of different sizes and structures is outlined. It is shown that these correlations are not necessarily negligible and should be taken into consideration when testing hypotheses concerning the mode of inheritance.
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Most models previously considered for assortative mating were such that no change in gene frequencies occurred, or that one-sided assortative mating was occurring. Two-sided assortative mating is more realistic for human populations, and in this paper a model of two-sided assortative mating is analysed for two autosomal alleles with dominance, an important case for human genetics. The concept of a relative probability of matin between two phenotypes is used, and this variable can take into account factors such as different propensities for assortment in the various phenotypes and so forth. It is shown that the gene frequency may vary from generation to generation and conditions for the establishment of a stable polymorphism are given. For instance, Stanton (1947) has considered a special case of two-sided assortative mating with two autosomal alleles and a constant correlation between mates, where the value expressed by the heterozygote is numerically exactly half-way between the values exhibited by the two homozygotes. Also he has considered a special form of assortative mating, where the probability of occurrence of matings between the same homozygotes has been increased in each generation by the same constant factor as the probability of occurrence of matings between different homozygotes has been decreased. The probability of occurrence of matings involving heterozygotes remains the same as if mating were random. For this particular model the frequency of the genotypes in those who mate in generation t is the same as for the general population in generation t, but the genotypic frequencies change from generation to generation, reaching an equilibrium value. Stark (1976) has also considered a similar model to Stanton's (1947), the major difference occurring in the construction of the mating frequencies, which in this case occurs according to the canonical decomposition of the 2-way table of mating frequencies. Stark shows the correspondence between the results for this model and those given by Malécot (1939, 1948). The results for all these models depend on the particular values assigned to the genotypes. Also these models could be extended as outlined in this article for the case of two autosomal alleles with dominance.
Nine cases of intrathoracic amyloid disease have been reviewed. A brief summary of historical material is presented along with detailed descriptions of the more pertinent cases. Observations suggest that a classification of the radiographic manifestations is needed with stress on massive calcific lymph node enlargement and a pulmonary lesion characterized by aggregations of small nodules.
Large samples results for the joint distribution of the gene frequency with the estimator for various measures of deviation from random mating are given. Also the difficulties in interpreting results for small samples are briefly discussed.
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