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Journal of Medical Genetics
|
January 1, 1996
Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease
J 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 samples
P Aula, K Raivio, S Autio
Human Genetics
|
July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4
K Grön, P Aula, L Peltonen
Developmental Medicine and Child Neurology
|
June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell disease
S Autio, P Aula, V Näntö
The Journal of Pediatrics
|
January 1, 1973
Enzyme defect in saccharopinuria
O Simell, T Johansson, P Aula
Neuropediatrics
|
November 1, 1980
Cry analysis of infants with karyotype abnormality
K 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
Page
of 17
Search research articles
Search
Showing results (31-40 of 161) with videos related to
Sort By:
Page
of 17
Journal of Medical Genetics
|
January 1, 1996
Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease
J 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 samples
P Aula, K Raivio, S Autio
Human Genetics
|
July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4
K Grön, P Aula, L Peltonen
Developmental Medicine and Child Neurology
|
June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell disease
S Autio, P Aula, V Näntö
The Journal of Pediatrics
|
January 1, 1973
Enzyme defect in saccharopinuria
O Simell, T Johansson, P Aula
Neuropediatrics
|
November 1, 1980
Cry analysis of infants with karyotype abnormality
K 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
Page
of 17