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D Bonneau

Showing results (81-90 of 143) with videos related to

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Journal of Medical Genetics|May 1, 1993
X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locusD Bonneau, J M Rozet, C Bulteau, et al.
Annales D'Endocrinologie|December 25, 2009
Hypochloremia and hyponatremia as the initial presentation of cystic fibrosis in three adultsM Priou-Guesdon, M-C Malinge, J-F Augusto, et al.
Nature Communications|August 7, 2015
Qubit entanglement between ring-resonator photon-pair sources on a silicon chipJ W Silverstone, R Santagati, D Bonneau, et al.
Nature Genetics|December 1, 1995
Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataractC Beaumont, P Leneuve, I Devaux, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Nature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.
Annales De Genetique|January 1, 1990
Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneityJ Kaplan, G Guasconi, D Bonneau, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Journal of Medical Genetics|January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH geneH Jacquet, J Berthelot, C Bonnemains, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|May 1, 1993
X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locusD Bonneau, J M Rozet, C Bulteau, et al.
Annales D'Endocrinologie|December 25, 2009
Hypochloremia and hyponatremia as the initial presentation of cystic fibrosis in three adultsM Priou-Guesdon, M-C Malinge, J-F Augusto, et al.
Nature Communications|August 7, 2015
Qubit entanglement between ring-resonator photon-pair sources on a silicon chipJ W Silverstone, R Santagati, D Bonneau, et al.
Nature Genetics|December 1, 1995
Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataractC Beaumont, P Leneuve, I Devaux, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Nature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.
Annales De Genetique|January 1, 1990
Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneityJ Kaplan, G Guasconi, D Bonneau, et al.
American Journal of Medical Genetics|September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and reviewD Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Journal of Medical Genetics|January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH geneH Jacquet, J Berthelot, C Bonnemains, et al.
Pageof 15