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Showing results (91-100 of 161) with videos related to

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American Journal of Human Genetics|June 1, 1991
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, P Aula, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1989
[Fabry's disease--a polymorphic generalized disease]E Nikoskelainen, M Penttinen, E Lindahl, et al.
Biochimica Et Biophysica Acta|July 17, 1992
Gene defects in Leber hereditary optic neuroretinopathyM L Savontaus, K Huoponen, A Majander, et al.
The Journal of Clinical Investigation|November 1, 1981
Cultured human amniotic fluid cells characterized with antibodies against intermediate filaments in indirect immunofluorescence microscopyI Virtanen, H von Koskull, V P Lehto, et al.
Obstetrics and Gynecology|June 1, 1981
Prenatal diagnosis of the Meckel syndromeO Karjalainen, P Aula, M Seppälä, et al.
Human Genetics|January 1, 1985
Improved technique for the expression of fragile-X in cultured amniotic fluid cellsH von Koskull, P Aula, P Ammälä, et al.
American Journal of Human Genetics|June 1, 1995
Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from FinlandM Hietala, A Hakonen, A R Aro, et al.
Clinical Chemistry|September 1, 1996
DNA-based carrier screening in primary healthcare: screening for aspartylglucosaminuria mutations in maternity health officesM Hietala, P Aula, A C Syvänen, et al.
Pediatric Research|November 1, 1980
Characterization of storage material in cultured fibroblasts by specific lectin binding in lysosomal storage diseasesI Virtanen, P Ekblom, P Laurila, et al.
Lancet (London, England)|July 17, 1976
Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoproteinM Seppälä, J Rapola, N P Huttunen, et al.
Pageof 17

Showing results (91-100 of 161) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|June 1, 1991
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, P Aula, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1989
[Fabry's disease--a polymorphic generalized disease]E Nikoskelainen, M Penttinen, E Lindahl, et al.
Biochimica Et Biophysica Acta|July 17, 1992
Gene defects in Leber hereditary optic neuroretinopathyM L Savontaus, K Huoponen, A Majander, et al.
The Journal of Clinical Investigation|November 1, 1981
Cultured human amniotic fluid cells characterized with antibodies against intermediate filaments in indirect immunofluorescence microscopyI Virtanen, H von Koskull, V P Lehto, et al.
Obstetrics and Gynecology|June 1, 1981
Prenatal diagnosis of the Meckel syndromeO Karjalainen, P Aula, M Seppälä, et al.
Human Genetics|January 1, 1985
Improved technique for the expression of fragile-X in cultured amniotic fluid cellsH von Koskull, P Aula, P Ammälä, et al.
American Journal of Human Genetics|June 1, 1995
Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from FinlandM Hietala, A Hakonen, A R Aro, et al.
Clinical Chemistry|September 1, 1996
DNA-based carrier screening in primary healthcare: screening for aspartylglucosaminuria mutations in maternity health officesM Hietala, P Aula, A C Syvänen, et al.
Pediatric Research|November 1, 1980
Characterization of storage material in cultured fibroblasts by specific lectin binding in lysosomal storage diseasesI Virtanen, P Ekblom, P Laurila, et al.
Lancet (London, England)|July 17, 1976
Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoproteinM Seppälä, J Rapola, N P Huttunen, et al.
Pageof 17