J Leisti|P Aula - JoVE Visualize

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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.

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.

Journal of Medical Genetics|June 27, 1998

New lethal disease involving type I and III collagen defect resembling geroderma osteodysplastica, De Barsy syndrome, and Ehlers-Danlos syndrome IVA Jukkola, S Kauppila, L Risteli, et al.

Annals of Medicine|April 1, 1990

Prenatal diagnosis of single gene disorders in northern FinlandJ Leisti, P Jouppila, A Mustonen, 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 (81-90 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.

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.

Journal of Medical Genetics|June 27, 1998

New lethal disease involving type I and III collagen defect resembling geroderma osteodysplastica, De Barsy syndrome, and Ehlers-Danlos syndrome IVA Jukkola, S Kauppila, L Risteli, et al.

Annals of Medicine|April 1, 1990

Prenatal diagnosis of single gene disorders in northern FinlandJ Leisti, P Jouppila, A Mustonen, 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.

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