Bjerkedal T, Irgens L M
Instituttgruppe for samfunnsmedisinske fag, Universitetet i Oslo.
Nord Med. 1993;108(8-9):211-2, 218.
Systematic monthly monitoring of the occurrence of congenital abnormalities has been practised in Norway since 1971, and has made important contributions in the field of perinatal epidemiology. The registry would also be a unique source of data for generation studies of reproductive outcome. Hitherto, little advantage has been taken of the possible uses of the registry for research into factors of importance to children's development, health and function. Important contributions can be made by using the registry in conjunction with other relevant registers within the health and social sectors. A research co-operation between the birth registers in the five Nordic countries was established in 1970.
自1971年以来，挪威一直对先天性异常的发生情况进行系统性月度监测，这在围产期流行病学领域做出了重要贡献。该登记册也是生殖结果代际研究的独特数据来源。迄今为止，该登记册在用于研究对儿童发育、健康和功能至关重要的因素方面，利用得很少。将该登记册与卫生和社会部门内的其他相关登记册结合使用，可以做出重要贡献。1970年，北欧五国的出生登记册之间建立了研究合作关系。
