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Clinical Genetics
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October 6, 2012
OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment
C Thauvin-Robinet, S Thomas, M Sinico, et al.
Journal of Medical Genetics
|
October 26, 2010
A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency
A S Lebre, M Rio, L Faivre d'Arcier, et al.
Clinical Genetics
|
March 16, 2017
Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations
N Lehman, A C Mazery, A Visier, et al.
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of 9
Search research articles
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Showing results (81-90 of 83) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 83 results.
Clinical Genetics
|
October 6, 2012
OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment
C Thauvin-Robinet, S Thomas, M Sinico, et al.
Journal of Medical Genetics
|
October 26, 2010
A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency
A S Lebre, M Rio, L Faivre d'Arcier, et al.
Clinical Genetics
|
March 16, 2017
Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations
N Lehman, A C Mazery, A Visier, et al.
Page
of 9