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Public health nurses (PHNs) can play an important role in the detection of domestic violence. This study examines whether the introduction of a domestic violence assessment protocol by public health nurses in a maternal and child health visiting program increases the identification and referral rates of women experiencing domestic violence. Data collected from case files during the baseline year prior to the initiation of the protocol were compared to case file information after the protocol had been implemented. When the protocol was used, there was a higher rate of identification, although the difference was not statistically significant. Significantly more women, however, were provided with information about domestic violence resources after the protocol was in place, and significantly more women were referred to services in the second year after the protocol had been implemented. This study provides support for the use of a domestic violence protocol to improve the public health nursing response to domestic violence.

A total of 2.7 X 10(6) chromosomes have been screened for deficiencies that extend into some portion of the 14A-15A segment of the X-chromosome. Mutants have been identified on the basis of their paralysis at high temperature (the para ts phenotype) in a stock which contains a para ts allele on the X-chromosome and a para+ allele on the Dp(1;4)r+f+ chromosome. Several hundred mutants have been genetically characterized and a large percentage are deficiencies. Cytological characterization of a sub-set suggests that breakpoints are distributed throughout the 14B-15A region, but in a non-random fashion.

The complementation pattern of twelve rudimentary mutations have been analyzed at two different levels. When analyzed on the basis of complementation for a wing abnormality the mutations can be divided into three groups, each of which is believed to affect the activity of one of the first three enzymes of pyrimidine synthesis (Norby, 1973; Jarry and Falk, 1974; Rawls and Fristrom, 1975). However, when the mutants are analyzed for complementation on the basis of a second phenotype, pyrimidine auxotrophy, the distinction between two of these three groups is not evident. The disparity in the two patterns probably reflects a different threshold of gene activity required for the detection of an auxotrophic phenotype as compared to that at which a wing abnormality is detectable. The biochemical basis of these results is interpreted in light of recent data suggesting that at least the first two enzymes of pyrimidine synthesis are contained within a single multifunctional protein complex (Soderholm et al., 1975).

In the previous paper of this series, a total of 446 mutations of the para gene were isolated following gamma- or X-irradiation. Of these, 180 were shown to be chromosome deficiencies. In this analysis we examine the molecular distribution of breakpoints in a subset of strains [38] which have an endpoint in the 14F-15A5 region. We find that although the breakpoints are distributed throughout the entire region, there is some regional specificity to the distribution of those endpoints.

The genetic and biochemical characteristics of a particular class of mutants at the rudimentary locus are described. The mutants are pyrimidine auxotrophs, like classical rudimentary alleles, but they are unique in that they do not alter the size or shape of the wing (Falk and Nash 1974b). Aspartate transcarbamylase and dihydroorotase activities have been measured in seven different normal-winged mutants, and the results indicate that these strains are enzymologically "leaky" mutants. Previous studies have shown that three genetic functions (corresponding to the first three enzymes of pyrimidine synthesis) are associated with the rudimentary locus. Four of the seven mutants appear to affect all three of these functions. Each of the four is temperature sensitive, and a biochemical analysis of the temperature sensitivity of one of these mutants, (r)pyr1-3, suggests that a process affecting the synthesis or assembly of these enzymes is altered at high temperatures.