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Lancet (London, England)|April 13, 1996
Prenatal diagnosis of Batten's diseaseP B Munroe, J Rapola, H M Mitchison, et al.Prenatal Diagnosis|May 1, 1991
DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)I Järvelä, J Rapola, L Peltonen, et al.Food Chemistry|August 10, 2024
Production and simulated digestion of high-load beads containing Schizochytrium oil encapsulated utilizing prilling techniqueGabriele Beltrame, Annelie Damerau, Eija Ahonen, et al.Kidney International|March 1, 1997
Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysisM Männikkö, M Kestilä, U Lenkkeri, et al.Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.Acta Psychiatrica Scandinavica|February 20, 2018
Smokin' hot: adolescent smoking and the risk of psychosisA Mustonen, T Ahokas, T Nordström, et al.Clinical Genetics|August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutationsM Encarnação, L Lacerda, R Costa, et al.Clinical Genetics|June 18, 2016
Identification of C12orf4 as a gene for autosomal recessive intellectual disabilityA K Philips, M Pinelli, C I de Bie, et al.Journal of Inherited Metabolic Disease|November 1, 2002
Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated familiesW J Kleijer, V H Garritsen, M Linnebank, et al.Journal of Medical Genetics|June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJ Dai, O-H Kim, T-J Cho, et al.Pageof 4