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Pharmacology & Toxicology|August 1, 1989
Prostaglandin F2 alpha binding to bovine ocular and synthetic melanins in vitroP Aula, T Kaila, R Huupponen, et al.Human Mutation|January 1, 1995
Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase geneA Isoniemi, M Hietala, P Aula, et al.Human Genetics|November 1, 1994
The fragile X syndrome in Finland: demonstration of a founder effect by analysis of microsatellite haplotypesR Haataja, M L Väisänen, M Li, et al.American Journal of Medical Genetics|January 1, 1988
A syndrome of multiple congenital contractures: neuropathological analysis on five fetal casesR Herva, N G Conradi, H Kalimo, 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.The Journal of Pediatrics|August 1, 1975
Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II)P Aula, J Rapola, S Autio, 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.Pageof 17