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Frans Hol

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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 mutationGretha 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 humansRiko Klootwijk, Pascal Groenen, Mascha Schijvenaars, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva 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 mutationsEva 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 neuropathyAn I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 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 mutationGretha 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 humansRiko Klootwijk, Pascal Groenen, Mascha Schijvenaars, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva 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 mutationsEva 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 neuropathyAn I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.
Pageof 1