Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nadine Pellen"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss S1, Pp 71-83 (2018)
Abstract Background The French Cystic Fibrosis Registry takes a census of the population of patients and records their annual data transmitted by Cystic Fibrosis Centers (CFCs). Quality of patient data has been a focus in the past years, with the imp
Externí odkaz:
https://doaj.org/article/f4db4371ac474927b403d8552a4e5e48
Autor:
Nadine Pellen, Tanguy Solliec
Publikováno v:
Studia Celto-Slavica. 12:63-104
This article was born out of two separate approaches carried out independently of one another. The first dealt with genetic demography and the second with variational linguistics, aiming to study the population and language of Brittany from a certain
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss S1, Pp 71-83 (2018)
Orphanet Journal of Rare Diseases, Vol 13, Iss S1, Pp 71-83 (2018)
Background The French Cystic Fibrosis Registry takes a census of the population of patients and records their annual data transmitted by Cystic Fibrosis Centers (CFCs). Quality of patient data has been a focus in the past years, with the implementati
Autor:
Nadine Pellen
Publikováno v:
La mucoviscidose en héritage ISBN: 9782733201831
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fb95375043e3033727f0baafc84e2fe
https://doi.org/10.4000/books.ined.1753
https://doi.org/10.4000/books.ined.1753
Autor:
Nadine Pellen
Publikováno v:
La mucoviscidose en héritage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57fcb3c1bfdf79ca1fc9fe67da9ac74f
https://doi.org/10.4000/books.ined.1743
https://doi.org/10.4000/books.ined.1743
Autor:
Nadine Pellen
Publikováno v:
La mucoviscidose en héritage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d153c1c851a422d4853aa2aad8f3996
https://doi.org/10.4000/books.ined.1733
https://doi.org/10.4000/books.ined.1733