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Scandinavian Audiology
|
January 1, 1982
The effect of age and hearing loss on the identification of synthetic /b, d, g/-stimuli
A Ginzel, C Brahe Pedersen, P E Spliid, et al.
Journal of the Neurological Sciences
|
September 15, 1996
Benign monomelic amyotrophies of upper and lower limb are not associated to deletions of survival motor neuron gene
G D Guglielmo, C Brahe, A Di Muzio, et al.
Amino Acids
|
July 20, 2000
Excitatory amino acid stimulation of the survival of rat cerebellar granule cells in culture is associated with an increase in SMN, the spinal muscular atrophy disease gene product
C Andreassi, A L Patrizi, C Brahe, et al.
Clinical Otolaryngology and Allied Sciences
|
April 1, 1984
Histiocytosis X. Recurrent otitis media as a presenting symptom in children with special references to cholesteatoma
A Coutté, C Brahe Pedersen, N Bartholdy, et al.
Biochemical Genetics
|
February 1, 1984
Catechol-O-methyltransferase: a method for autoradiographic visualization of isozymes in cellogel
C Brahe, N Crosti, P Meera Khan, et al.
Scandinavian Audiology
|
January 1, 1982
The role of temporal factors in auditory perception of consonants and vowels. A study of different age groups
A Ginzel, C Brahe Pedersen, P E Spliid, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Potential gene sequence isolation and regional mapping in human chromosome 21
C Brahe, F Tassone, A Millington-Ward, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 1, 1997
Human COL6A1: genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2
D Trikka, T Davis, V Lapenta, et al.
Human Genetics
|
November 1, 1986
Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybrids
C Brahe, P Bannetta, P Meera Khan, et al.
Lancet (London, England)
|
September 16, 1995
Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy
C Brahe, S Servidei, S Zappata, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
Scandinavian Audiology
|
January 1, 1982
The effect of age and hearing loss on the identification of synthetic /b, d, g/-stimuli
A Ginzel, C Brahe Pedersen, P E Spliid, et al.
Journal of the Neurological Sciences
|
September 15, 1996
Benign monomelic amyotrophies of upper and lower limb are not associated to deletions of survival motor neuron gene
G D Guglielmo, C Brahe, A Di Muzio, et al.
Amino Acids
|
July 20, 2000
Excitatory amino acid stimulation of the survival of rat cerebellar granule cells in culture is associated with an increase in SMN, the spinal muscular atrophy disease gene product
C Andreassi, A L Patrizi, C Brahe, et al.
Clinical Otolaryngology and Allied Sciences
|
April 1, 1984
Histiocytosis X. Recurrent otitis media as a presenting symptom in children with special references to cholesteatoma
A Coutté, C Brahe Pedersen, N Bartholdy, et al.
Biochemical Genetics
|
February 1, 1984
Catechol-O-methyltransferase: a method for autoradiographic visualization of isozymes in cellogel
C Brahe, N Crosti, P Meera Khan, et al.
Scandinavian Audiology
|
January 1, 1982
The role of temporal factors in auditory perception of consonants and vowels. A study of different age groups
A Ginzel, C Brahe Pedersen, P E Spliid, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Potential gene sequence isolation and regional mapping in human chromosome 21
C Brahe, F Tassone, A Millington-Ward, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 1, 1997
Human COL6A1: genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2
D Trikka, T Davis, V Lapenta, et al.
Human Genetics
|
November 1, 1986
Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybrids
C Brahe, P Bannetta, P Meera Khan, et al.
Lancet (London, England)
|
September 16, 1995
Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy
C Brahe, S Servidei, S Zappata, et al.
Page
of 5