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M Rio

Showing results (71-80 of 107) with videos related to

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Journal of Medical Genetics|April 5, 2003
Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?V Cormier-Daire, F Molinari, M Rio, et al.
Mitochondrion|February 25, 2020
Expanding the phenotype of mitochondrial disease: Novel pathogenic variant in ISCA1 leading to instability of the iron-sulfur cluster in the proteinE Lebigot, M Hully, L Amazit, et al.
Mbio|June 6, 2019
Mutualist-Provisioned Resources Impact Vector CompetencyRita V M Rio, Anna K S Jozwick, Amy F Savage, et al.
Epidemiology and Infection|October 1, 1996
Prevalence and characteristics of Escherichia coli serotype O157:H7 and other verotoxin-producing E. coli in healthy cattleM Blanco, J E Blanco, J Blanco, et al.
Journal of Medical Genetics|December 14, 2004
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndromeG Borck, R Redon, D Sanlaville, et al.
Journal of Medical Genetics|May 6, 2014
Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlationsM Bricout, D Grévent, A S Lebre, et al.
Revue Neurologique|April 29, 2014
[Aspect of brain MRI in mitochondrial respiratory chain deficiency. A diagnostic algorithm of the most common mitochondrial genetic mutations]M Devaux-Bricout, D Grévent, A-S Lebre, et al.
Human Reproduction (Oxford, England)|January 5, 2001
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and menJ Gekas, F Thepot, C Turleau, et al.
Nanotechnology|August 5, 2009
The cellular uptake of meta-tetra(hydroxyphenyl)chlorin entrapped in organically modified silica nanoparticles is mediated by serum proteinsChiara Compagnin, Luca Baù, Maddalena Mognato, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|April 5, 2003
Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?V Cormier-Daire, F Molinari, M Rio, et al.
Mitochondrion|February 25, 2020
Expanding the phenotype of mitochondrial disease: Novel pathogenic variant in ISCA1 leading to instability of the iron-sulfur cluster in the proteinE Lebigot, M Hully, L Amazit, et al.
Mbio|June 6, 2019
Mutualist-Provisioned Resources Impact Vector CompetencyRita V M Rio, Anna K S Jozwick, Amy F Savage, et al.
Epidemiology and Infection|October 1, 1996
Prevalence and characteristics of Escherichia coli serotype O157:H7 and other verotoxin-producing E. coli in healthy cattleM Blanco, J E Blanco, J Blanco, et al.
Journal of Medical Genetics|December 14, 2004
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndromeG Borck, R Redon, D Sanlaville, et al.
Journal of Medical Genetics|May 6, 2014
Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlationsM Bricout, D Grévent, A S Lebre, et al.
Revue Neurologique|April 29, 2014
[Aspect of brain MRI in mitochondrial respiratory chain deficiency. A diagnostic algorithm of the most common mitochondrial genetic mutations]M Devaux-Bricout, D Grévent, A-S Lebre, et al.
Human Reproduction (Oxford, England)|January 5, 2001
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and menJ Gekas, F Thepot, C Turleau, et al.
Nanotechnology|August 5, 2009
The cellular uptake of meta-tetra(hydroxyphenyl)chlorin entrapped in organically modified silica nanoparticles is mediated by serum proteinsChiara Compagnin, Luca Baù, Maddalena Mognato, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Pageof 11