Zobrazeno 1 - 10
of 614
pro vyhledávání: '"poirier"'
Autor:
Wertheim, L. Jon
Publikováno v:
Sports Illustrated. Oct2021, Vol. 132 Issue 11, p46-51. 6p. 5 Color Photographs.
Autor:
Poirier, Jean-Marie
Publikováno v:
Lute Society of America Quarterly. Spring2017, Vol. 52 Issue 1, p17-25. 9p.
Autor:
Poirier, Mark Jude
Publikováno v:
Georgia Review. Fall2021, Vol. 75 Issue 3, p755-767. 13p.
Autor:
Tanselle, G. Thomas
Publikováno v:
Raritan. Spring2010, Vol. 29 Issue 4, p187-202. 16p.
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
The Poirier-Bienvenu neurodevelopmental syndrome (POBINDS) is a rare disease caused by mutations in the CSNK2B gene, which is characterized by intellectual disability and early-onset epilepsy. Mosaicism has not been previously reported in CSNK2B gene
Externí odkaz:
https://doaj.org/article/9040995c4c61428689a55cac492c26b6
Autor:
Bühler, Birgit, Kirchengast, Sylvia
Publikováno v:
Anthropological Review. 85(3):67-82
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=1073480
Autor:
White, Owen1
Publikováno v:
French Colonial History. 2019, Vol. 18, p129-154. 26p.
Autor:
Poirier, Richard
Publikováno v:
Raritan. Spring90, Vol. 9 Issue 4, p14. 18p.
Autor:
Prasida Unni, Jack Friend, Janice Weinberg, Volkan Okur, Jennifer Hochscherf, Isabel Dominguez
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Okur-Chung Neurodevelopmental Syndrome (OCNDS) and Poirier-Bienvenu Neurodevelopmental Syndrome (POBINDS) were recently identified as rare neurodevelopmental disorders. OCNDS and POBINDS are associated with heterozygous mutations in the CSNK2A1 and C
Externí odkaz:
https://doaj.org/article/a9a3d5b0648b46458f328d3b63f24f1e
Autor:
Pedersen, Nils Arne1 (AUTHOR) teonap@cas.au.dk
Publikováno v:
Vigiliae Christianae. 2019, Vol. 73 Issue 4, p463-468. 6p.