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P Aula

Showing results (31-40 of 161) with videos related to

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Journal of Medical Genetics|January 1, 1996
Haplotype analysis in prenatal diagnosis and carrier identification of Salla diseaseJ Schleutker, P Sistonen, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|February 8, 2002
[The claw hand: first sign of a metabolic disease]M Penttinen, T Aärimaa, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1971
[Intrauterine diagnosis of a chromosome translocation]P Aula, O Karjalainen, J Leisti
Pediatric Research|June 1, 1976
Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samplesP Aula, K Raivio, S Autio
Human Genetics|July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4K Grön, P Aula, L Peltonen
Developmental Medicine and Child Neurology|June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell diseaseS Autio, P Aula, V Näntö
The Journal of Pediatrics|January 1, 1973
Enzyme defect in saccharopinuriaO Simell, T Johansson, P Aula
Neuropediatrics|November 1, 1980
Cry analysis of infants with karyotype abnormalityK Michelsson, N Tuppurainen, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1984
[Should parents be informed of fetal sex following genetic amniocentesis?]L Vaara, P Aula, O Karjalainen
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1975
[Amniotic fluid analysis in the early diagnosis of fetal abnormalities]P Aula, O Karjalainen, M Seppälä
Pageof 17

Showing results (31-40 of 161) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|January 1, 1996
Haplotype analysis in prenatal diagnosis and carrier identification of Salla diseaseJ Schleutker, P Sistonen, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|February 8, 2002
[The claw hand: first sign of a metabolic disease]M Penttinen, T Aärimaa, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1971
[Intrauterine diagnosis of a chromosome translocation]P Aula, O Karjalainen, J Leisti
Pediatric Research|June 1, 1976
Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samplesP Aula, K Raivio, S Autio
Human Genetics|July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4K Grön, P Aula, L Peltonen
Developmental Medicine and Child Neurology|June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell diseaseS Autio, P Aula, V Näntö
The Journal of Pediatrics|January 1, 1973
Enzyme defect in saccharopinuriaO Simell, T Johansson, P Aula
Neuropediatrics|November 1, 1980
Cry analysis of infants with karyotype abnormalityK Michelsson, N Tuppurainen, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1984
[Should parents be informed of fetal sex following genetic amniocentesis?]L Vaara, P Aula, O Karjalainen
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1975
[Amniotic fluid analysis in the early diagnosis of fetal abnormalities]P Aula, O Karjalainen, M Seppälä
Pageof 17