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C Raynal

Showing results (31-40 of 36) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 28, 2017
Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screeningI Sermet-Gaudelus, J Brouard, M-P Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 4, 2018
Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR geneA Bergougnoux, K Délétang, A Pommier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 5, 2017
[Management of infants whose diagnosis is inconclusive at neonatal screening for cystic fibrosis]I Sermet-Gaudelus, J Brouard, M-P Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 2, 2017
Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutationC Guissart, C Dubucs, C Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022
The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 20, 2024
ECFS standards of care on CFTR-related disorders: Identification and care of the disordersN J Simmonds, K W Southern, E De Wachter, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 28, 2017
Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screeningI Sermet-Gaudelus, J Brouard, M-P Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 4, 2018
Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR geneA Bergougnoux, K Délétang, A Pommier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 5, 2017
[Management of infants whose diagnosis is inconclusive at neonatal screening for cystic fibrosis]I Sermet-Gaudelus, J Brouard, M-P Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 2, 2017
Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutationC Guissart, C Dubucs, C Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022
The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 20, 2024
ECFS standards of care on CFTR-related disorders: Identification and care of the disordersN J Simmonds, K W Southern, E De Wachter, et al.
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