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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.Journal of Mental Deficiency Research|December 1, 1986
Screening of inherited oligosaccharidurias among mentally retarded patients in northern FinlandP Aula, M Renlund, K O Raivio, et al.Journal of Biochemistry|October 1, 1975
Characterization of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU)K Sugahara, S Funakoshi, I Funakoshi, et al.Human Genetics|January 1, 1984
Identification of cells from fetal bladder epithelium in human amniotic fluidH von Koskull, P Aula, L K Trejdosiewicz, et al.The Journal of Clinical Endocrinology and Metabolism|July 9, 2004
Effect of multiple endocrine neoplasia type 1 (MEN1) gene mutations on premature mortality in familial MEN1 syndrome with founder mutationsT Ebeling, O Vierimaa, S Kytölä, et al.Cancer|January 1, 1988
Familial occurrence of malignant lymphoepithelial lesion of the parotid gland in a Finnish family with dominantly inherited trichoepitheliomaH Autio-Harmainen, P Pääkkö, M Alavaikko, et al.Pediatrics|April 1, 1992
Fumarase deficiency: two siblings with enlarged cerebral ventricles and polyhydramnios in uteroA M Remes, H Rantala, J K Hiltunen, et al.Acta Neuropathologica|January 1, 1995
Familial fetal akinesia deformation sequence with a skeletal muscle maturation defectK Vuopala, F Pedrosa-Domellöf, R Herva, 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.Pageof 17