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P Aula

Showing results (121-130 of 161) with videos related to

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Birth Defects Original Article Series|January 1, 1974
The phenotype of human triploidyJ T Leisti, K O Raivio, M H Rapola, et al.
Human Genetics|September 1, 1997
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritanceK Silander, P Meretoja, H Pihko, et al.
Genomics|March 1, 1992
Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in FinlandA C Syvänen, E Ikonen, T Manninen, et al.
Infectious Diseases of Poverty|August 7, 2023
Optimisation of the DNA dipstick as a rapid extraction method for Schistosoma japonicum in infected mice samples and spiked human clinical samplesOyime P Aula, Donald P McManus, Malcolm K Jones, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
British Journal of Obstetrics and Gynaecology|May 1, 1983
Antenatal screening for congenital nephrosis in Finland by maternal serum alpha-fetoproteinM Ryynänen, M Seppälä, P Kuusela, et al.
British Medical Journal|November 29, 1980
Glial origin of rapidly adhering amniotic fluid cellsP Aula, H von Koskull, K Teramo, et al.
Monographs in Human Genetics|January 1, 1978
Four patients with a new lysosomal storage disorder (Salla disease)P Aula, K Raivio, S Autio, et al.
Human Genetics|September 1, 1995
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy numberM Laan, K Grön-Virta, A Salo, et al.
Pageof 17

Showing results (121-130 of 161) with videos related to

Sort By:
Pageof 17
Birth Defects Original Article Series|January 1, 1974
The phenotype of human triploidyJ T Leisti, K O Raivio, M H Rapola, et al.
Human Genetics|September 1, 1997
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritanceK Silander, P Meretoja, H Pihko, et al.
Genomics|March 1, 1992
Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in FinlandA C Syvänen, E Ikonen, T Manninen, et al.
Infectious Diseases of Poverty|August 7, 2023
Optimisation of the DNA dipstick as a rapid extraction method for Schistosoma japonicum in infected mice samples and spiked human clinical samplesOyime P Aula, Donald P McManus, Malcolm K Jones, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
British Journal of Obstetrics and Gynaecology|May 1, 1983
Antenatal screening for congenital nephrosis in Finland by maternal serum alpha-fetoproteinM Ryynänen, M Seppälä, P Kuusela, et al.
British Medical Journal|November 29, 1980
Glial origin of rapidly adhering amniotic fluid cellsP Aula, H von Koskull, K Teramo, et al.
Monographs in Human Genetics|January 1, 1978
Four patients with a new lysosomal storage disorder (Salla disease)P Aula, K Raivio, S Autio, et al.
Human Genetics|September 1, 1995
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy numberM Laan, K Grön-Virta, A Salo, et al.
Pageof 17