Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Aula

Showing results (81-90 of 161) with videos related to

Pageof 17
Sort By:
Prenatal Diagnosis|September 1, 1989
First-trimester prenatal diagnosis of aspartylglucosaminuriaP Aula, K Mattila, O Piiroinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Carnitine deficiency and severe nausea-induced thiamine deficiency causing a metabolic crisis]V Salonen, J Nikoskelainen, O J Heinonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.
Prenatal Diagnosis|April 1, 1982
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in Meckel's syndrome: a new test for prenatal diagnosis?M Heikinheimo, P Aula, J Rapola, et al.
British Medical Journal (Clinical Research Ed.)|August 11, 1984
Risk of minor and major fetal malformations in diabetics with high haemoglobin A1c values in early pregnancyK Ylinen, P Aula, U H Stenman, et al.
Human Genetics|January 1, 1992
Exclusion map of Salla disease: attempts to localize the disease gene using a computer programL Haataja, J Schleutker, M Renlund, et al.
American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.
The Journal of Clinical Investigation|April 1, 1991
Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharidesG M Mancini, C E Beerens, P P Aula, et al.
Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.
American Journal of Human Genetics|March 1, 1991
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7J Vilkki, J Ott, M L Savontaus, et al.
Pageof 17

Showing results (81-90 of 161) with videos related to

Sort By:
Pageof 17
Prenatal Diagnosis|September 1, 1989
First-trimester prenatal diagnosis of aspartylglucosaminuriaP Aula, K Mattila, O Piiroinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Carnitine deficiency and severe nausea-induced thiamine deficiency causing a metabolic crisis]V Salonen, J Nikoskelainen, O J Heinonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.
Prenatal Diagnosis|April 1, 1982
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in Meckel's syndrome: a new test for prenatal diagnosis?M Heikinheimo, P Aula, J Rapola, et al.
British Medical Journal (Clinical Research Ed.)|August 11, 1984
Risk of minor and major fetal malformations in diabetics with high haemoglobin A1c values in early pregnancyK Ylinen, P Aula, U H Stenman, et al.
Human Genetics|January 1, 1992
Exclusion map of Salla disease: attempts to localize the disease gene using a computer programL Haataja, J Schleutker, M Renlund, et al.
American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.
The Journal of Clinical Investigation|April 1, 1991
Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharidesG M Mancini, C E Beerens, P P Aula, et al.
Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.
American Journal of Human Genetics|March 1, 1991
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7J Vilkki, J Ott, M L Savontaus, et al.
Pageof 17