The inheritance of palmar pattern ridge counts for individual palmar areas, combined distal areas, and all ten areas combined was investigated in families belonging to two strictly endogamous Brahmin castes of peninsular India. Ridge count phenotypes were obtained by the method proposed by Malhotra et al. (1981a), however, zero observations (indicating patterns not circumscribed by triradii) were excluded from analysis. Path analytic methods were applied in order to determine the relative influences of polygenes, intrauterine environment, and residual environment. The proportion of genetic variation was, in general, consistently greater in one population than the other, and significant intrauterine environmental effects were detected for the population with lower heritabilities. The results of this investigation suggest that a simple polygenic model may not be sufficient to explain the inheritance of ridge counts in the interdigital IV configurational area. Distal pattern ridge counts do not appear to be influenced by more or less uterine environmental effects than all areas considered together. The proportion of genetic variation for the total palmar pattern ridge count was 52% in both populations.

Maximum likelihood estimates of familial correlations are presented for 12 cranio-facial measurements taken on 399 nuclear families from Southern India. Marital resemblance is significantly different from zero for head circumference, head breadth, minimum frontal breadth, bizygomatic breadth, total facial height, and nasal height, but not for bigonial breadth, nose breadth, nose depth, or ear dimensions. All other familial correlations are significantly greater than zero except for the father-daughter correlation for nasal depth. Path analysis with a TAU transmission model with sex effects reveals that family resemblance for head circumference, head length, bigonial breadth, total facial height, and nasal height, but not for bigonial breadth, nose breadth, nose depth, or ear dimensions. All other familial correlations are significantly greater than zero except for the father-daughter correlation for nasal depth. Path analysis with a TAU transmission model with sex effects breadth, and sex effects in transmission were found for head breadth and nose dimensions. Sex effects in this sample may be due to the fact that different anthropometrists were used for male and female subjects.

Path analysis of 12 cranio-facial measurements from a sample of nuclear families and twins from Andhra Pradesh, India is used to test hypotheses about the familial transmission of these traits. For bigonial breadth and ear dimensions, the transmission from parent to child is consistent with simple autosomal polygenic inheritance, but length, breadth and circumference of the head, facial breadth and nose dimensions show evidence of transmission in excess of polygenic expectations. Additional non-transmissible resemblance of sibling pairs is not significant for any of the variables, but twin pairs do exhibit significant additional resemblance for head circumference, head length, minimum frontal breadth, bizygomatic breadth and ear dimensions. The effect of interobserver measurement differences can be detected for head breadth, minimum frontal breadth, bigonial breadth, total facial height and nose dimensions.

The heritability of sole pattern ridge counts was examined in two family studies of endogamous castes from peninsular India. The phenotypes included ridge counts for each of the eight configurational areas separately, all areas combined, and only distal areas combined. Differences in heritability estimates were found between populations as well as among the individual configurational areas. Although some ridge counts do not show familial resemblance, others appear to be moderately heritable. Estimates of h2 range from 0.36 to 0.63 in one family series and from 0.22 to 0.51 in the other. In addition, significant uterine environmental effects were detected in one family series but not in the other.