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P Aula

Showing results (101-110 of 161) with videos related to

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Neuromuscular Disorders : NMD|February 3, 1998
Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western FinlandP Meretoja, K Silander, H Kalimo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Salla disease - a new inherited Finnish disease]P Aula, M Renlund, K Raivio, et al.
Developmental Neuroscience|January 1, 1991
Sialic acid storage disorders: observations on clinical and biochemical variationG M Mancini, F W Verheijen, C E Beerens, et al.
Human Genetics|October 1, 1993
The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathyK Huoponen, T Lamminen, V Juvonen, et al.
Human Mutation|January 1, 1997
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathyV Juvonen, E Nikoskelainen, T Lamminen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1996
[Attitudes toward genetic testing in Finland]P Aula, M Hietala, P Niemelä, et al.
American Journal of Diseases of Children (1960)|October 1, 1978
Prenatal diagnosis of congenital nephrosis in 23 high-risk familiesP Aula, J Rapola, O Karjalainen, et al.
Clinical Genetics|October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosisA de la Chapelle, E M Sankila, M Lindlöf, et al.
Human Genetics|November 1, 1991
Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla diseaseJ Schleutker, L Haataja, M Renlund, et al.
Prenatal Diagnosis|October 1, 1981
Glial and neuronal cells in amniotic fluid of anencephalic pregnanciesH von Koskull, I Virtanen, V P Lehto, et al.
Pageof 17

Showing results (101-110 of 161) with videos related to

Sort By:
Pageof 17
Neuromuscular Disorders : NMD|February 3, 1998
Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western FinlandP Meretoja, K Silander, H Kalimo, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Salla disease - a new inherited Finnish disease]P Aula, M Renlund, K Raivio, et al.
Developmental Neuroscience|January 1, 1991
Sialic acid storage disorders: observations on clinical and biochemical variationG M Mancini, F W Verheijen, C E Beerens, et al.
Human Genetics|October 1, 1993
The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathyK Huoponen, T Lamminen, V Juvonen, et al.
Human Mutation|January 1, 1997
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathyV Juvonen, E Nikoskelainen, T Lamminen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1996
[Attitudes toward genetic testing in Finland]P Aula, M Hietala, P Niemelä, et al.
American Journal of Diseases of Children (1960)|October 1, 1978
Prenatal diagnosis of congenital nephrosis in 23 high-risk familiesP Aula, J Rapola, O Karjalainen, et al.
Clinical Genetics|October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosisA de la Chapelle, E M Sankila, M Lindlöf, et al.
Human Genetics|November 1, 1991
Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla diseaseJ Schleutker, L Haataja, M Renlund, et al.
Prenatal Diagnosis|October 1, 1981
Glial and neuronal cells in amniotic fluid of anencephalic pregnanciesH von Koskull, I Virtanen, V P Lehto, et al.
Pageof 17