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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 13, 2007
Resting muscle pain as the first clinical symptom in children carrying the MTTK A8344G mutation
Gretha van de Glind, Maaike de Vries, Richard Rodenburg, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Genetic variants in ZIC1, ZIC2, and ZIC3 are not major risk factors for neural tube defects in humans
Riko Klootwijk, Pascal Groenen, Mascha Schijvenaars, et al.
American Journal of Medical Genetics. Part A
|
February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome
Eva Morava, Richard Rodenburg, Frans Hol, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2006
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations
Eva Morava, Richard J Rodenburg, Frans Hol, et al.
BMJ Case Reports
|
June 21, 2011
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
An I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 13, 2007
Resting muscle pain as the first clinical symptom in children carrying the MTTK A8344G mutation
Gretha van de Glind, Maaike de Vries, Richard Rodenburg, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Genetic variants in ZIC1, ZIC2, and ZIC3 are not major risk factors for neural tube defects in humans
Riko Klootwijk, Pascal Groenen, Mascha Schijvenaars, et al.
American Journal of Medical Genetics. Part A
|
February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome
Eva Morava, Richard Rodenburg, Frans Hol, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2006
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations
Eva Morava, Richard J Rodenburg, Frans Hol, et al.
BMJ Case Reports
|
June 21, 2011
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
An I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.
Page
of 1