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Prenatal Diagnosis
|
March 1, 1984
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in fetal developmental disorders
M Heikinheimo, H Jalanko, J Leisti, et al.
Neurology
|
January 1, 1983
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism
M Renlund, P Aula, K O Raivio, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1991
[Molecular genetics of aspartylglucosaminuria]
L Palotie, E Ikonen, A C Syvänen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 15, 1991
Spectrum of mutations in aspartylglucosaminuria
E Ikonen, P Aula, K Grön, et al.
Social Science & Medicine (1982)
|
July 17, 1998
Attitudes towards genetic testing: analysis of contradictions
P Jallinoja, A Hakonen, A R Aro, et al.
American Journal of Human Genetics
|
June 1, 1997
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14
T Lauteala, P Sistonen, M L Savontaus, et al.
Human Mutation
|
January 1, 1994
Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy
K Huoponen, V Juvonen, A Iitiä, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy
T Lamminen, K Huoponen, P Sistonen, et al.
American Journal of Human Genetics
|
August 19, 2000
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation
N Aula, P Salomäki, R Timonen, et al.
Archives of Neurology
|
February 1, 1979
"Salla disease": a new lysosomal storage disorder
P Aula, S Autio, K O Raivio, et al.
Page
of 17
Search research articles
Search
Showing results (131-140 of 161) with videos related to
Sort By:
Page
of 17
Prenatal Diagnosis
|
March 1, 1984
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in fetal developmental disorders
M Heikinheimo, H Jalanko, J Leisti, et al.
Neurology
|
January 1, 1983
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism
M Renlund, P Aula, K O Raivio, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1991
[Molecular genetics of aspartylglucosaminuria]
L Palotie, E Ikonen, A C Syvänen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 15, 1991
Spectrum of mutations in aspartylglucosaminuria
E Ikonen, P Aula, K Grön, et al.
Social Science & Medicine (1982)
|
July 17, 1998
Attitudes towards genetic testing: analysis of contradictions
P Jallinoja, A Hakonen, A R Aro, et al.
American Journal of Human Genetics
|
June 1, 1997
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14
T Lauteala, P Sistonen, M L Savontaus, et al.
Human Mutation
|
January 1, 1994
Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy
K Huoponen, V Juvonen, A Iitiä, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy
T Lamminen, K Huoponen, P Sistonen, et al.
American Journal of Human Genetics
|
August 19, 2000
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation
N Aula, P Salomäki, R Timonen, et al.
Archives of Neurology
|
February 1, 1979
"Salla disease": a new lysosomal storage disorder
P Aula, S Autio, K O Raivio, et al.
Page
of 17