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D Bonneau

Showing results (71-80 of 143) with videos related to

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Clinical Genetics|December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1P Amati-Bonneau, L Pasquier, E Lainey, et al.
Human Genetics|July 1, 1991
Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotypeD Bonneau, J L Huret, G Godeau, et al.
Surgery|June 1, 1997
Familial papillary carcinoma of the thyroidJ L Kraimps, M H Bouin-Pineau, P Amati, et al.
Computer Methods in Biomechanics and Biomedical Engineering|July 31, 2014
In vivo cervical intervertebral disc characterisation by elastographyC Vergari, P Rouch, G Dubois, et al.
American Journal of Human Genetics|May 1, 1996
A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23P Amati, P Gasparini, J Zlotogora, et al.
Computer Methods in Biomechanics and Biomedical Engineering|June 27, 2012
Subject-specific musculoskeletal model of the lower limb in a lying and standing positionJ Hausselle, A Assi, A El Helou, et al.
Therapie|January 1, 1993
Medications exposure during pregnancy. A study in a university hospitalM Berthier, D Bonneau, M C Perault, et al.
Molecular and Cellular Biochemistry|November 4, 1992
Blockade of insulin sensitive steady-state R-type Ca2+ channel by PN 200-110 in heart and vascular smooth muscleG Bkaily, D Economos, L Potvin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 14, 2004
Prenatal diagnosis of absence of the septum pellucidum associated with septo-optic dysplasiaC Lepinard, R Coutant, F Boussion, et al.
Journal of Medical Genetics|November 6, 2009
Phenotypic spectrum of MFN2 mutations in the Spanish populationC Casasnovas, I Banchs, J Cassereau, et al.
Pageof 15

Showing results (71-80 of 143) with videos related to

Sort By:
Pageof 15
Clinical Genetics|December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1P Amati-Bonneau, L Pasquier, E Lainey, et al.
Human Genetics|July 1, 1991
Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotypeD Bonneau, J L Huret, G Godeau, et al.
Surgery|June 1, 1997
Familial papillary carcinoma of the thyroidJ L Kraimps, M H Bouin-Pineau, P Amati, et al.
Computer Methods in Biomechanics and Biomedical Engineering|July 31, 2014
In vivo cervical intervertebral disc characterisation by elastographyC Vergari, P Rouch, G Dubois, et al.
American Journal of Human Genetics|May 1, 1996
A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23P Amati, P Gasparini, J Zlotogora, et al.
Computer Methods in Biomechanics and Biomedical Engineering|June 27, 2012
Subject-specific musculoskeletal model of the lower limb in a lying and standing positionJ Hausselle, A Assi, A El Helou, et al.
Therapie|January 1, 1993
Medications exposure during pregnancy. A study in a university hospitalM Berthier, D Bonneau, M C Perault, et al.
Molecular and Cellular Biochemistry|November 4, 1992
Blockade of insulin sensitive steady-state R-type Ca2+ channel by PN 200-110 in heart and vascular smooth muscleG Bkaily, D Economos, L Potvin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 14, 2004
Prenatal diagnosis of absence of the septum pellucidum associated with septo-optic dysplasiaC Lepinard, R Coutant, F Boussion, et al.
Journal of Medical Genetics|November 6, 2009
Phenotypic spectrum of MFN2 mutations in the Spanish populationC Casasnovas, I Banchs, J Cassereau, et al.
Pageof 15