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Pierre-Antoine Rollat-Farnier

Showing results (1-10 of 23) with videos related to

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DNA and Cell Biology|January 25, 2021
Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency?Louis Januel, Valérie Chanavat, Pierre-Antoine Rollat-Farnier, et al.
Genome Biology and Evolution|April 12, 2014
The genome of Cardinium cBtQ1 provides insights into genome reduction, symbiont motility, and its settlement in Bemisia tabaciDiego Santos-Garcia, Pierre-Antoine Rollat-Farnier, Francisco Beitia, et al.
European Journal of Medical Genetics|February 21, 2022
Disruption and deletion of the proximal part of TCF4 are associated with mild intellectual disability: About three new patientsJulie Masson, Linda Pons, Tiffany Busa, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 4, 2021
Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia AYohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Human Mutation|November 16, 2019
Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathyAlexandre Janin, Valérie Chanavat, Pierre-Antoine Rollat-Farnier, et al.
European Journal of Medical Genetics|September 29, 2019
A 14q distal chromoanagenesis elucidated by whole genome sequencingFlavie Ader, Solveig Heide, Pauline Marzin, et al.
Molecular Syndromology|October 12, 2019
Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the <i>ELN</i> Gene Uncovered by Whole-Genome SequencingLinda Pons, Patrice Bouvagnet, Mohamed Bakloul, et al.
BMC Genomics|April 19, 2015
Genome reduction and potential metabolic complementation of the dual endosymbionts in the whitefly Bemisia tabaciQiong Rao, Pierre-Antoine Rollat-Farnier, Dan-Tong Zhu, et al.
Orphanet Journal of Rare Diseases|June 2, 2019
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum DisorderJulie Masson, Caroline Demily, Nicolas Chatron, et al.
Genome Biology and Evolution|February 26, 2015
Two host clades, two bacterial arsenals: evolution through gene losses in facultative endosymbiontsPierre-Antoine Rollat-Farnier, Diego Santos-Garcia, Qiong Rao, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

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Pageof 3
DNA and Cell Biology|January 25, 2021
Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency?Louis Januel, Valérie Chanavat, Pierre-Antoine Rollat-Farnier, et al.
Genome Biology and Evolution|April 12, 2014
The genome of Cardinium cBtQ1 provides insights into genome reduction, symbiont motility, and its settlement in Bemisia tabaciDiego Santos-Garcia, Pierre-Antoine Rollat-Farnier, Francisco Beitia, et al.
European Journal of Medical Genetics|February 21, 2022
Disruption and deletion of the proximal part of TCF4 are associated with mild intellectual disability: About three new patientsJulie Masson, Linda Pons, Tiffany Busa, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 4, 2021
Complete characterisation of two new large Xq28 duplications involving F8 using whole genome sequencing in patients without haemophilia AYohann Jourdy, Claire Bardel, Mathilde Fretigny, et al.
Human Mutation|November 16, 2019
Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathyAlexandre Janin, Valérie Chanavat, Pierre-Antoine Rollat-Farnier, et al.
European Journal of Medical Genetics|September 29, 2019
A 14q distal chromoanagenesis elucidated by whole genome sequencingFlavie Ader, Solveig Heide, Pauline Marzin, et al.
Molecular Syndromology|October 12, 2019
Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the <i>ELN</i> Gene Uncovered by Whole-Genome SequencingLinda Pons, Patrice Bouvagnet, Mohamed Bakloul, et al.
BMC Genomics|April 19, 2015
Genome reduction and potential metabolic complementation of the dual endosymbionts in the whitefly Bemisia tabaciQiong Rao, Pierre-Antoine Rollat-Farnier, Dan-Tong Zhu, et al.
Orphanet Journal of Rare Diseases|June 2, 2019
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum DisorderJulie Masson, Caroline Demily, Nicolas Chatron, et al.
Genome Biology and Evolution|February 26, 2015
Two host clades, two bacterial arsenals: evolution through gene losses in facultative endosymbiontsPierre-Antoine Rollat-Farnier, Diego Santos-Garcia, Qiong Rao, et al.
Pageof 3