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The American Journal of Pathology|January 1, 1985
Extracellular matrix and epithelial differentiation of Wilms' tumorH Sariola, P Ekblom, J Rapola, et al.
Archives of Disease in Childhood|July 1, 1986
Disturbed calcium and phosphate homeostasis during treatment with ACTH of infantile spasmsR Riikonen, O Simell, J Jääskeläinen, et al.
Clinical Genetics|September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildrenM Kähkönen, J Leisti, C J Thoden, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Prospects of carrier screening of aspartylglucosaminuria in FinlandM Hietala, K Grön, A C Syvänen, et al.
Prenatal Diagnosis|September 1, 1989
First-trimester prenatal diagnosis of aspartylglucosaminuriaP Aula, K Mattila, O Piiroinen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.
Ophthalmology|December 1, 1985
Gyrate atrophy of the choroid and retina. A five-year follow-up of creatine supplementationK Vannas-Sulonen, I Sipilä, A Vannas, et al.
European Heart Journal|December 1, 1993
Altered serum lipid profile after systemic infection in children: risk factor for CHD?E Pesonen, J Rapola, J Viikari, et al.
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