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P Aula

Showing results (71-80 of 161) with videos related to

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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.
Annals of Clinical Research|August 1, 1979
Safety and accuracy of midtrimester amniocentesis for prenatal diagnosis of genetic disordersP Aula, O Karjalainen, K Teramo, 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.
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.
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.
American Journal of Human Genetics|July 1, 1993
Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)V Juvonen, J Vilkki, P Aula, et al.
Pageof 17

Showing results (71-80 of 161) with videos related to

Sort By:
Pageof 17
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.
Annals of Clinical Research|August 1, 1979
Safety and accuracy of midtrimester amniocentesis for prenatal diagnosis of genetic disordersP Aula, O Karjalainen, K Teramo, 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.
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.
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.
American Journal of Human Genetics|July 1, 1993
Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)V Juvonen, J Vilkki, P Aula, et al.
Pageof 17