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Gut|December 1, 1980
Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhoodI Kosnai, P Kuitunen, E Savilahti, et al.Pathology, Research and Practice|June 1, 1990
Cell differentiation in sacrococcygeal teratomas. An immunohistochemical and follow-up studyP Lahdenne, M Heikinheimo, M Perkkiö, et al.Journal of the Neurological Sciences|December 1, 1992
Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophyB Udd, J Rapola, P Nokelainen, et al.Human Genetics|January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndromeA de la Chapelle, R Herva, M Koivisto, et al.Prenatal Diagnosis|October 1, 1983
Alkaline phosphatase activity in amniotic fluid in pregnancies with fetal disordersH Jalanko, M Heikinheimo, M Ryynänen, et al.Prenatal Diagnosis|May 22, 2001
Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine familiesP Salomäki, N Aula, V Juvonen, et al.Journal of Biochemistry|November 1, 1977
Structure of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU)K Sugahara, M Akasaki, I Funakoshi, et al.Genomics|October 1, 1996
A physical map of the 6q14-q15 region harboring the locus for the lysosomal membrane sialic acid transport defectP Leppänen, J Isosomppi, J Schleutker, et al.American Journal of Human Genetics|November 1, 1984
Assignment of the structural gene encoding human aspartylglucosaminidase to the long arm of chromosome 4 (4q21----4qter)P Aula, K H Astrin, U Francke, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Pregnancy-specific beta-1-glycoprotein (SP1) in cultured amniotic fluid cellsM Heikinheimo, T Wahlström, P Aula, et al.Pageof 27