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D Bonneau

Showing results (91-100 of 143) with videos related to

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Journal of Medical Genetics|July 5, 2003
Visceral manifestations in hereditary haemorrhagic telangiectasia type 2S A Abdalla, U W Geisthoff, D Bonneau, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Human Molecular Genetics|December 1, 1994
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patientsP Miniou, M Jeanpierre, V Blanquet, et al.
Journal of Medical Genetics|January 1, 1996
Evidence for a fourth locus in Usher syndrome type IS Gerber, D Larget-Piet, J M Rozet, et al.
Applied Optics|November 19, 2010
Dispersed fringe tracking with the multi-r(0) apertures of the Grand Interféromètre à 2 TélescopesL Koechlin, P R Lawson, D Mourard, et al.
European Journal of Neurology|October 19, 2007
Cognitive changes in asymptomatic carriers of the Huntington disease mutation geneC Verny, P Allain, A Prudean, et al.
American Journal of Human Genetics|December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2F Canzian, P Amati, H R Harach, et al.
Journal of Medical Genetics|August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locusP Edery, A Pelet, L M Mulligan, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
Journal of Medical Genetics|December 1, 1995
No evidence of genetic heterogeneity in dominant optic atrophyD Bonneau, E Souied, S Gerber, et al.
Pageof 15

Showing results (91-100 of 143) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|July 5, 2003
Visceral manifestations in hereditary haemorrhagic telangiectasia type 2S A Abdalla, U W Geisthoff, D Bonneau, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Human Molecular Genetics|December 1, 1994
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patientsP Miniou, M Jeanpierre, V Blanquet, et al.
Journal of Medical Genetics|January 1, 1996
Evidence for a fourth locus in Usher syndrome type IS Gerber, D Larget-Piet, J M Rozet, et al.
Applied Optics|November 19, 2010
Dispersed fringe tracking with the multi-r(0) apertures of the Grand Interféromètre à 2 TélescopesL Koechlin, P R Lawson, D Mourard, et al.
European Journal of Neurology|October 19, 2007
Cognitive changes in asymptomatic carriers of the Huntington disease mutation geneC Verny, P Allain, A Prudean, et al.
American Journal of Human Genetics|December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2F Canzian, P Amati, H R Harach, et al.
Journal of Medical Genetics|August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locusP Edery, A Pelet, L M Mulligan, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
Journal of Medical Genetics|December 1, 1995
No evidence of genetic heterogeneity in dominant optic atrophyD Bonneau, E Souied, S Gerber, et al.
Pageof 15