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American Journal of Preventive Medicine|September 1, 1986
Effects of labeling and treatment of hypertension on perceived healthL C Harlan, B F Polk, S Cooper, et al.
American Journal of Epidemiology|January 1, 1984
Disability days associated with detection and treatment in a hypertension control programB F Polk, L C Harlan, S P Cooper, et al.
The British Journal of Dermatology|November 11, 2010
Multiple miliary osteoma cutis is a distinct disease entity: four case reports and review of the literatureR M Myllylä, K M Haapasaari, R Palatsi, et al.
American Journal of Human Genetics|July 31, 1998
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsP Mäkelä-Bengs, N Järvinen, K Vuopala, et al.
The Journal of Cell Biology|August 1, 1990
Molecular cloning of the rat integrin alpha 1-subunit: a receptor for laminin and collagenM J Ignatius, T H Large, M Houde, et al.
Human Mutation|June 20, 1998
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathiesK Silander, P Meretoja, V Juvonen, et al.
Clinical Genetics|June 29, 2017
A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron lossT Paakkola, K Vuopala, H Kokkonen, et al.
American Journal of Human Genetics|October 27, 1997
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationE Laiho, J Ignatius, H Mikkola, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Expression of apolipoprotein E during nerve degeneration and regenerationM J Ignatius, P J Gebicke-Härter, J H Skene, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
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