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Biochemical Medicine and Metabolic Biology
|
August 1, 1993
Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase
R Halila, E Ikonen, O Tollersrud, et al.
DNA and Cell Biology
|
March 1, 1994
Dissection of the molecular consequences of a double mutation causing a human lysosomal disease
A Riikonen, E Ikonen, R Sormunen, et al.
Applied Optics
|
November 25, 2010
Improved frequency stability of an external cavity diode laser by eliminating temperature and pressure effects
H Talvitie, J Aman, H Ludvigsen, et al.
American Journal of Obstetrics and Gynecology
|
December 1, 1984
Prenatal diagnosis and treatment of fetal thyrotoxicosis
F Pekonen, K Teramo, T Mäkinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1986
[Huntington's disease]
J Palo, H Somer, L Palotie, et al.
Optics Express
|
June 25, 2009
Realization of two Fourier-limited solid-state single-photon sources
R Lettow, V Ahtee, R Pfab, et al.
Genomics
|
March 1, 1992
Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland
A C Syvänen, E Ikonen, T Manninen, et al.
The Journal of Cell Biology
|
September 1, 1995
Intracellular routing of wild-type and mutated polymeric immunoglobulin receptor in hippocampal neurons in culture
M de Hoop, C von Poser, C Lange, et al.
Clinical Endocrinology
|
July 1, 1984
Antithyroid treatment of maternal hyperthyroidism during lactation
B A Lamberg, E Ikonen, K Osterlund, et al.
Acta Endocrinologica
|
June 1, 1981
Treatment of maternal hyperthyroidism with antithyroid agents and changes in thyrotrophin and thyroxine in the newborn
B A Lamberg, E Ikonen, K Teramo, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 91) with videos related to
Sort By:
Page
of 10
Biochemical Medicine and Metabolic Biology
|
August 1, 1993
Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase
R Halila, E Ikonen, O Tollersrud, et al.
DNA and Cell Biology
|
March 1, 1994
Dissection of the molecular consequences of a double mutation causing a human lysosomal disease
A Riikonen, E Ikonen, R Sormunen, et al.
Applied Optics
|
November 25, 2010
Improved frequency stability of an external cavity diode laser by eliminating temperature and pressure effects
H Talvitie, J Aman, H Ludvigsen, et al.
American Journal of Obstetrics and Gynecology
|
December 1, 1984
Prenatal diagnosis and treatment of fetal thyrotoxicosis
F Pekonen, K Teramo, T Mäkinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1986
[Huntington's disease]
J Palo, H Somer, L Palotie, et al.
Optics Express
|
June 25, 2009
Realization of two Fourier-limited solid-state single-photon sources
R Lettow, V Ahtee, R Pfab, et al.
Genomics
|
March 1, 1992
Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland
A C Syvänen, E Ikonen, T Manninen, et al.
The Journal of Cell Biology
|
September 1, 1995
Intracellular routing of wild-type and mutated polymeric immunoglobulin receptor in hippocampal neurons in culture
M de Hoop, C von Poser, C Lange, et al.
Clinical Endocrinology
|
July 1, 1984
Antithyroid treatment of maternal hyperthyroidism during lactation
B A Lamberg, E Ikonen, K Osterlund, et al.
Acta Endocrinologica
|
June 1, 1981
Treatment of maternal hyperthyroidism with antithyroid agents and changes in thyrotrophin and thyroxine in the newborn
B A Lamberg, E Ikonen, K Teramo, et al.
Page
of 10