Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Thibaut Kuntz"'
Autor:
Virginie Laugel-Haushalter, Marie Paschaki, Pauline Marangoni, Coralie Pilgram, Arnaud Langer, Thibaut Kuntz, Julie Demassue, Supawich Morkmued, Philippe Choquet, André Constantinesco, Fabien Bornert, Matthieu Schmittbuhl, Solange Pannetier, Laurent Viriot, André Hanauer, Pascal Dollé, Agnès Bloch-Zupan
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e84343 (2014)
BackgroundThe RSK2 gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental retardation, skeletal growth delays, with craniofacial and digital abnormalities typically associated with this syndrome. Craniofac
Externí odkaz:
https://doaj.org/article/59354c677b234ef4aa0e1bfbf8185d97
Autor:
Coralie Pilgram, Laurent Viriot, Marie Paschaki, Solange Pannetier, Agnès Bloch-Zupan, Pascal Dollé, Philippe Choquet, A. Constantinesco, André Hanauer, Julie Demassue, Virginie Laugel-Haushalter, Arnaud Langer, Fabien Bornert, Thibaut Kuntz, Matthieu Schmittbuhl, Supawich Morkmued, Pauline Marangoni
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e84343 (2014)
PLoS ONE
PLoS ONE
BackgroundThe RSK2 gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental retardation, skeletal growth delays, with craniofacial and digital abnormalities typically associated with this syndrome. Craniofac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96dacf3a7abab575e32b490bdeb48f8b
https://doi.org/10.1371/journal.pone.0084343
https://doi.org/10.1371/journal.pone.0084343