In 773 three-generation families of twins, individual probability of nonrighthandedness (NRH) depends significantly on the handedness of that individual's parents. The parents of twins are much more often NRH than are their nontwinbearing siblings. The twins and their siblings apparently inherit the excess liability for NRH shown by their parents. Monozygotic (MZ) pairs are significantly about twice as often concordant (casewise) for handedness as dizygotic (DZ) pairs. Overall, the best-fitting mode of transmission is autosomal, NRH dominant to RH with penetrance of about 50% in the heterozygote, or multifactorial, with heritability of 60–70%. Under the major-gene approach, heterogeneity seems likely, with about one-third of the families showing no NRH outside of the twin sibships. MZ/DZ concordance ratio is about four in those families, suggestive of recessive inheritance. A 1.16-fold excess of NRH in twins compared to their siblings, and a 1.8-fold excess in the second-born members of same-sex discordant pairs, leaves open the possibility that a minor portion of NRH in twins may be secondary to transient hypoxia and/or acidosis.

The condition of low birth weight is compared in twins and in singletons in terms of birth weight distributions and with respect to factors such as the incidence of sillbirths, length of gestation, maternal age, parity, and legitimacy. In the light of demographic, biological, and developmental considerations, it is concluded that low birth weight in twins is a different condition from low birth weight in singletons and should be dealt with independently, especially in view of the different implications for child growth and survival.

Self-reported cold data have been analyzed for 95 pairs of identical twins aged 14–64 who took part in a double-blind trial of vitamin C tablets. One member of each twin pair took a tablet containing 1 g vitamin C and the other took a well-matched placebo each day for 100 days. In the total sample there was no effect of vitamin C in preventing colds. However, subdivision of the data showed a significant preventive effect of the placebo in the 51 pairs living together and an equal and opposite preventive effect of the vitamin C in the 44 pairs living apart. The placebo effect in the pairs living together may be attributed to the large proportion who wrongly perceived which treatment they were taking. The reduction of colds in the vitamin C group of the pairs living apart was about 20%. There were significant correlations between cold symptoms reported and the personality trait of neuroticism. No side effects or substantive changes in serum biochemistry could be attributed to the vitamin C dose.

A statistical model and analysis for genetic and environmental effects in twin-family data are presented. The model is used to derive expressions for phenotypic correlations of 22 essential pair relationships in twin-family units. The analysis proceeds in two steps. First, differential effects of sex, generation, and sex-zygosity of twin-family units and correlations due to cluster sampling are eliminated from correlation data. Then, estimates and tests of model parameters are calculated from the adjusted data. The theory and methods were developed for a Swedish twin-family study of many behaviors possibly related to the smoking habit. There, it is important to screen for behaviors that clearly are under genetic control and to assess relative influences of various biological and social environments on the development of all behaviors. Height data from the Swedish study are used to illustrate concepts and methods presented in this paper.

The expected correlation between polar body twins depends upon the frequency and distribution of chiasmata occurring during oogenesis. We have estimated the expected values of these correlations using assumptions believed to be biologically valid. The expected value of the overall correlation between first polar body twins is estimated to be 0.38 and that between second polar body twins is estimated to be 0.51. There is little difference between the correlation of DZ twins and that expected for second polar body twins.

The correlation for a specific locus depends upon its distance from the centromere for both types of polar body twins. This effect is especially marked for second polar body twins. For second polar body twins, loci at or near the telomere will have a correlation close to that expected for first polar body twins. It is concluded that only those marker genes that lie at or close to the centromere are appropriate for the detection of polar body twinning.

In a study carried out in an African population in Western Nigeria and a Caucasian population in Aberdeen, Scotland, it was found that DZ twinning rates varied with maternal age and parity, the MZ twinning rate remaining fairly constant. However, women aged 30–34 were found to have the highest rate in Western Nigeria whereas the peak in Aberdeen population occurred in the older age group, 35–39 years. Other factors that influenced DZ twinning rates were maternal height, social class and ethnicity (in the Nigerian population), and illegitimacy (in the Aberdeen population). No significant association was found between twinning and maternal blood groups or season of the year in either of the two populations. An important factor that also influenced twinning in the two populations was the maternal serum FSH level. The levels were much higher in the Nigerian population than in the Aberdeen population. Furthermore, in the Aberdeen population, twin-prone and non-twin-prone women had similar serum FSH levels, whereas the levels were much higher in twin-prone women in the Nigerian population. This finding is consistent with the fact that the Nigerian population has a much higher twinning incidence (approximately 50 per 1,000 maternities) than Aberdeen population (approximately 12 per 1,000 maternities).

The application of multiway contingency table analysis to the multivariate analysis of concordance ratios in twin studies is developed. The approach is illustrated by data on smoking and alcohol use in Finland and Sweden. This approach can enable the assessment of the effect of other variables on the concordance ratio and thus allow estimates of genetic effects on the trait under study. Hypotheses on relationships between genetic effects and other variables can be tested. After hypothesis testing, model fitting of the best hypothesis can be carried out.

An evaluation of the maternal effect on spontaneous abortion and the genetic contribution to various reproductive variables was made using like-sexed twins born between 1915–1946. Health and reproductive questionnaires were sent to 2,365 twin pairs listed in the Norwegian Twin Registry. Zygosity was determined by a questionnaire which proved to be 98% accurate in discriminating between monozygotic (MZ) and dizygotic (DZ) twins. Verification of the zygosity questionnaire was accomplished by blood cell marker zygosity determination in 200 twin pairs. Data from 428 monozygotic twin pairs (174 male pairs and 254 female pairs) were analyzed by a new model for qualitative traits and a striking maternal effect was found. The results suggested that over 54% of all women may belong to a high risk group who have approximately a 13% risk of early fetal loss. The incidence of first trimester abortions and spontaneous abortion reported by a sample of 915 like-sexed twin pairs and spouses was .079 and .089, respectively; there were no significant differences between male and female pairs.

Other reproductive variables were studied in both MZ and DZ twins including the age of menarche and menopause, the age at marriage and birth of the first child, and the interval between marriage and the first birth. These variables were examined for evidence of genetic effects and secular trends. The mean age of menarche had decreased significantly between the years 1915–1935 and 1936–1946. The secular trend appeared to be environmental in nature and accounted for more than 7% of the overall variation in age of menarche. Sixty-five percent of the variation in the age of menarche was attributed to genetic factors. The mean age of marriage and the mean age at the first birth decreased significantly between 1915–1935 and 1936–1946. Twins born between 1936–1946 also reported fewer pregnancies than did twins born between 1915–1946, but this was statistically significant among MZ twins only; no significant difference in the frequency of spontaneous abortions was found between the 1915–1935 and the 1936–1946 groups.

Although there were occasional groups in which differences were statistically significant, no general trends were identified in comparing couples who reported a spontaneous abortion with those who did not. Traits compared were: the age of menarche, age of marriage, age at first birth, the interval between marriage and first birth and the mean present age of the twins and spouses. Couples reporting a first trimester spontaneous abortion had significantly more total pregnancies than those not reporting a spontaneous abortion. Unaffected pregnancies were also significantly more numerous in couples with a spontaneous abortion compared to those without, suggesting over-compensation for fetal loss.

A maternal effect in spontaneous abortion was indicated by the correlation coefficients found; significant positive correlations were found in both MZ and DZ females but not in males. For total pregnancies and unaffected pregnancies, MZ twins, both male and female, had significant correlation coefficients while DZ twins did not.

Sixteen pairs of term discordant twins (weight discrepancy of more than 20% when the, lighter twin was compared to the heavier) were evaluated at birth. Weight, length, head circumference, anterior fontanel area, and combined ossification of the knee epiphyses were measured, and ponderal index (weight/length ratio) calculated. The most severely growth retarded infants had markedly decreased ossification and larger anterior fontanels.

Eleven pairs had physical measurements at one year of age. With individual exceptions, the lighter twins at birth remained smaller in all dimensions. Despite these persistent differences between twin pairs, the values for length at one year of age were within normal limits for both the heavier and lighter twins. Infants without ossification at birth had a greater incremental linear growth by one year than those infants with ossification.

Patterns of NOR activity in 640 metaphase spreads from twelve monozygotic (MZ) and eight dizygotic (DZ) twin pairs were studied to evaluate the heritability of this chromosomal heteromorphism. NORs were stained by a modification of the Ag-AS technique and counterstained with quinacrine mustard dihydrochloride to facilitate chromosome identification and assess their value in zygosity determination. In this study, all karyotypes were read blind with respect to zygosity and pair membership.

A discriminant function analysis of pair score differences in MZ and DZ twins revealed that, in our sample, the probability of accurately determining zygosity with NOR scores was 0.93 and with QFQ scores was 0.99. We conclude that NOR and QFQ scores are highly heritable and of great value in zygosity determination.

Data were collected from 687 metaphase spreads on the frequency with which an acrocentric chromosome was found in a satellite association. A significant correlation was found between this frequency and the degree of Ag-AS stain of the NOR. This study, therefore, confirms previous results showing that a high degree of NOR activity is found in those chromosomes most often involved in satellite associations.

Taste threshold for phenylthiocarbamide (PTC) was measured in 393 offspring from the families of 85 monozygotic (MZ) twin pairs. PTC scores were bimodally distributed with modes at one and eight and the antimode at five. Because of the non-normality of the distribution, a jackknife procedure was used to obtain 95% confidence intervals for the estimates of genetic, maternal, and environmental parameters. Analyses which assumed no epistasis and which included additive genetic effects revealed that 37.9% of the observed variation in PTC threshold was due to additive genetic effects, 16.6% was due to dominance effects, 14.2% was due to maternal effects, 13.7% was due to a common sibship environment, and 17.6% was due to random environmental effects, yielding a broad sense heritability of 0.55 for the threshold ability to taste PTC. Analyses which did not include additive genetic effects revealed 26.6% of the observed variance was due to dominance effects, 23.6% to maternal effects, and 49.8% to environmental effects at the 0.67 confidence levels, but that environmental factors accounted for 72.4% and dominance effects for 23.6% of the observed variation at the 95% level.

The rates of infant mortality of twin individuals were 4.38% and 7.76% for mothers healthy and nonhealthy after delivery, respectively, and the difference is significant at the 0.01 level. The lowest infant mortality rate was seen in the mothers with paid work during pregnancy (4.56%), followed by the mothers engaged only in housekeeping (4.72%) and by those self-employed during the pregnancy (4.99%). Infant mortality rate for MZ twins decreased with increased monthly expenditure of the household, whereas the rate for DZ twins remained constant with expenditure. Socioeconomic factors still affect the infant mortality of twins, and the infant mortality rate can be improved.

A total of 71 pairs of like-sexed dizygotic twins were studied, comparing within-pair differences for plasma total, free and esterified cholesterol, and triglyceride with the number of HLA haplotypes the twins had in common. If associations are present between HLA and the blood lipids studied, the twins with no haplotypes in common would be expected to have the largest within-pair mean square, those with two in common the smallest, and those with one in common an intermediate value. No significant differences were found comparing within-pair mean squares for the variables studied.

A statistical index is proposed in order to determine twin zygosity based on weight and height measures and a Bayesian test of hypotheses. Some Roman twin data are analyzed on the basis of the Euclidean distance index, which appears to be the best for an easy calculation and for its genetic interpretation based on the formulation of genetic distance.

The inheritance of total ridge count (TRC) was studied in 967 individuals from the families of 111 pairs of MZ twins. The sample included data on 47 male half-sibships with 227 offspring and 64 female half-sibships with 306 offspring. The males in this sample had a mean ridge count of 135 ± 2 and the females a mean ridge count of 124 ± 2. The distribution of scores for females showed evidence for significant skewness. For this reason, prior to the analysis, the data were corrected for sex and adjusted to normality using a power transformation. Nested analyses of variance were performed on the ridge counts from male and female half-sibships separately to derive estimates of among, between, and within-variance components. These estimates were then used in a nonlinear least squares program to estimate genetic and environmental parameters and to determine the goodness of fit of various models. A model which included additive genetic and dominance effects could not be rejected (P = 0.67) but did not fit the data as well as a simple additive genetic-random environmental model (P = 0.81). The addition of maternal effects to the latter model also provided a satisfactory fit (P = 0.68). However, there was no improvement in the goodness of fit over the simple model, and the estimated magnitude of the maternal effect was not significantly different from zero.

The rate of infant mortality of triplet individuals (deaths under one year of age) was computed using 34 sets of triplets born in the first half of 1974. The rates were 8.82%, 9.68%, and 10.34% for the first-, second-, and the third-born triplets, respectively. For males and females the rates were 8.33% and 10.34%, respectively, and the difference was not significant. The rate decreased with gestational age up to 32-35 weeks. For those with heavier weight at birth (≤2,000 g) the rate was lower (0%) than for those with lighter weight (<2,000 g, 8.16%), but the difference is not significant (P = 0.087). Infant mortality rate of triplets decreased with increased monthly expenditure of the household.