Search research articles
Contact Us
Filters
Showing results (11-20 of 20) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 20 results.
Journal of Medical Genetics
|
January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutation
K Ravn, J B Nielsen, P Uldall, et al.
American Journal of Medical Genetics
|
June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosis
H H Goebel, F Gullotta, T Bajanowski, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome
K Ravn, F Wibrand, F J Hansen, et al.
Der Nervenarzt
|
August 19, 2007
[Integrated treatment of depression in Aachen]
T Kirchner, F Bergmann, J Engels, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
February 17, 2000
Gait disturbance interpreted as cerebellar ataxia after MMR vaccination at 15 months of age: a follow-up study
A M Plesner, F J Hansen, K Taudorf, et al.
Human Molecular Genetics
|
January 1, 1997
Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophy
M Schwartz, N Sørensen, F J Hansen, et al.
International Disability Studies
|
April 1, 1990
The handicap code of the ICIDH, adapted for children aged 6-7 years. Classification Group of the Nordic Neuropediatric Association
J Diderichsen, H Ferngren, F J Hansen, et al.
Ugeskrift for Laeger
|
October 15, 1998
[Guidelines on antiepileptic treatment of children]
P V Uldall, F J Hansen, B Beck, et al.
Human Molecular Genetics
|
October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion
J Poulton, K Morten, C Freeman-Emmerson, et al.
Neuromuscular Disorders : NMD
|
November 1, 1995
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis
C Wallgren-Pettersson, K Avela, S Marchand, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Journal of Medical Genetics
|
January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutation
K Ravn, J B Nielsen, P Uldall, et al.
American Journal of Medical Genetics
|
June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosis
H H Goebel, F Gullotta, T Bajanowski, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome
K Ravn, F Wibrand, F J Hansen, et al.
Der Nervenarzt
|
August 19, 2007
[Integrated treatment of depression in Aachen]
T Kirchner, F Bergmann, J Engels, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
February 17, 2000
Gait disturbance interpreted as cerebellar ataxia after MMR vaccination at 15 months of age: a follow-up study
A M Plesner, F J Hansen, K Taudorf, et al.
Human Molecular Genetics
|
January 1, 1997
Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophy
M Schwartz, N Sørensen, F J Hansen, et al.
International Disability Studies
|
April 1, 1990
The handicap code of the ICIDH, adapted for children aged 6-7 years. Classification Group of the Nordic Neuropediatric Association
J Diderichsen, H Ferngren, F J Hansen, et al.
Ugeskrift for Laeger
|
October 15, 1998
[Guidelines on antiepileptic treatment of children]
P V Uldall, F J Hansen, B Beck, et al.
Human Molecular Genetics
|
October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion
J Poulton, K Morten, C Freeman-Emmerson, et al.
Neuromuscular Disorders : NMD
|
November 1, 1995
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis
C Wallgren-Pettersson, K Avela, S Marchand, et al.
Page
of 2