Author:
Kääriäinen Helena,Muilu Juha,Perola Markus,Kristiansson Kati
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology
Reference49 articles.
1. Aalto-Setälä K, Viikari J, Åkerblom HK, Kuusela V, Kontula K (1991) DNA polymorphims of the apolipoprotein B and A-I/C-III-genes are associated with variations of serum low density lipoprotein cholesterol level in childhood. J Lipid Res 32:1477–1487
2. Aula P, Astrin KH, Francke U, Desnick RJ (1984) Assignment of the structural gene encoding human aspartylglucosaminidase to the long arm of chromosome 4 (4q21-4qter). Am J Hum Genet 36:1215–1224
3. Autti-Rämö I, Mäkelä M, Sintonen H, Koskinen H, Laajalahti L, Halila R, Kääriäinen H, Lapatto R, Näntö-Salonen K, Pulkki K, Renlund M, Salo M, Tyni T (2005) Expanding screening for rare metabolic disease in the newborn: an analysis of costs, effect and ethical consequences for decision-making in Finland. Acta Paediatr 94:1126–1136
4. Brandt-Rauf SI, Raveis VH, Drummond NF, Conte JA, Rothman SM (2006) Ashkenazi Jews and breast cancer: the consequences of linking ethnic identity to genetic disease. Am J Public Health 96:1979–1988. doi: 10.2105/AJPH.2005.083014
5. Cao A, Rosatelli MC, Monni G, Galanello R (2002) Screening for thalassemia. A model of success. Obstet Gynekol Clin N Am 29:305–328
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