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Nature|August 17, 1995
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosisJ Vesa, E Hellsten, L A Verkruyse, et al.
British Journal of Haematology|September 1, 1989
Characterization of neoplastic and reactive cells in T-cell lymphomas with cytogenetic, surface marker, and DNA methodsC Lindholm, K O Franssila, L Teerenhovi, et al.
Human Genetics|July 1, 1997
Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intoleranceT Lauteala, N Horelli-Kuitunen, E Closs, et al.
The Journal of Infectious Diseases|August 1, 1995
Osteitis caused by bacille Calmette-Guérin vaccination: a retrospective analysis of 222 casesL Kröger, M Korppi, E Brander, 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.
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.
Archives of Biochemistry and Biophysics|December 1, 1988
Pyrazole is different from acetone and ethanol as an inducer of the polysubstrate monooxygenase system in mice: evidence that pyrazole-inducible P450Coh is distinct from acetone-inducible P450acP Honkakoski, S Autio, R Juvonen, et al.
Neuropediatrics|March 8, 2000
Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI studyT Autti, J Rapola, P Santavuori, 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.
American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.
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