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P Aula

Showing results (61-70 of 161) with videos related to

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Prenatal Diagnosis|March 1, 1994
Transabdominal chorionic villus sampling and amniocentesis for prenatal diagnosis: 5 years' experience at a university centreP Palo, O Piiroinen, E Honkonen, et al.
Pharmacology & Toxicology|August 1, 1989
Prostaglandin F2 alpha binding to bovine ocular and synthetic melanins in vitroP Aula, T Kaila, R Huupponen, et al.
Human Mutation|January 1, 1995
Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase geneA Isoniemi, M Hietala, P Aula, et al.
American Journal of Obstetrics and Gynecology|November 15, 1977
Prenatal diagnosis of the Meckel syndromeP Aula, O Karjalainen, J Rapola, et al.
Human Genetics|January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndromeA de la Chapelle, R Herva, M Koivisto, et al.
Prenatal Diagnosis|October 1, 1983
Alkaline phosphatase activity in amniotic fluid in pregnancies with fetal disordersH Jalanko, M Heikinheimo, M Ryynänen, et al.
The Journal of Pediatrics|August 1, 1975
Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II)P Aula, J Rapola, S Autio, et al.
Archives of Disease in Childhood|April 1, 1973
Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18J Leisti, S Leisti, J Perheentupa, et al.
FEBS Letters|June 15, 1977
Structural studies of glycoasparagines from urine of a patient with aspartylglycosylaminuria (AGU)K Sugahara, M Akasaki, I Funakoshi, et al.
Prenatal Diagnosis|May 22, 2001
Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine familiesP Salomäki, N Aula, V Juvonen, et al.
Pageof 17

Showing results (61-70 of 161) with videos related to

Sort By:
Pageof 17
Prenatal Diagnosis|March 1, 1994
Transabdominal chorionic villus sampling and amniocentesis for prenatal diagnosis: 5 years' experience at a university centreP Palo, O Piiroinen, E Honkonen, et al.
Pharmacology & Toxicology|August 1, 1989
Prostaglandin F2 alpha binding to bovine ocular and synthetic melanins in vitroP Aula, T Kaila, R Huupponen, et al.
Human Mutation|January 1, 1995
Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase geneA Isoniemi, M Hietala, P Aula, et al.
American Journal of Obstetrics and Gynecology|November 15, 1977
Prenatal diagnosis of the Meckel syndromeP Aula, O Karjalainen, J Rapola, et al.
Human Genetics|January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndromeA de la Chapelle, R Herva, M Koivisto, et al.
Prenatal Diagnosis|October 1, 1983
Alkaline phosphatase activity in amniotic fluid in pregnancies with fetal disordersH Jalanko, M Heikinheimo, M Ryynänen, et al.
The Journal of Pediatrics|August 1, 1975
Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II)P Aula, J Rapola, S Autio, et al.
Archives of Disease in Childhood|April 1, 1973
Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18J Leisti, S Leisti, J Perheentupa, et al.
FEBS Letters|June 15, 1977
Structural studies of glycoasparagines from urine of a patient with aspartylglycosylaminuria (AGU)K Sugahara, M Akasaki, I Funakoshi, et al.
Prenatal Diagnosis|May 22, 2001
Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine familiesP Salomäki, N Aula, V Juvonen, et al.
Pageof 17