Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yvette Macary"'
Autor:
Marion Imbert-Bouteille, Carole Corsini, Marie-Christine Picot, Lucas Mizrahy, Sandrine Akouete, Helena Huguet, Frédéric Thomas, David Geneviève, Patrice Taourel, Marc Ychou, Virginie Galibert, Chloé Rideau, Karen Baudry, Tatiana Kogut Kubiak, Isabelle Coupier, Rémy Hobeika, Yvette Macary, Alain Toledano, Jérôme Solassol, Antoine Maalouf, Jean-Pierre Daures, Pascal Pujol
Publikováno v:
Genes, Vol 12, Iss 7, p 1100 (2021)
According to clinical guidelines, the occurrence of very early-onset breast cancer (VEO-BC) (diagnosed ≤ age 30 years) or VEO ovarian cancer (VEO-OC) (diagnosed ≤ age 40 years) in families with BRCA1 or BRCA2 mutation (BRCAm) prompts advancing th
Externí odkaz:
https://doaj.org/article/d6823048128045799adbe5d88e11e39f
Autor:
Tatiana Kogut Kubiak, Marc Ychou, Lucas Mizrahy, Jérôme Solassol, Carole Corsini, Virginie Galibert, Sandrine Akouete, Marion Imbert-Bouteille, Karen Baudry, David Geneviève, Antoine Maalouf, Pascal Pujol, Patrice Taourel, Remy Hobeika, Chloé Rideau, Frédéric Thomas, Helena Huguet, Yvette Macary, Alain Toledano, Jean-Pierre Daurès, Isabelle Coupier, Marie-Christine Picot
Publikováno v:
Genes
Genes, 2021, 12 (7), pp.1100. ⟨10.3390/genes12071100⟩
Genes, Vol 12, Iss 1100, p 1100 (2021)
Volume 12
Issue 7
Genes, 2021, 12 (7), pp.1100. ⟨10.3390/genes12071100⟩
Genes, Vol 12, Iss 1100, p 1100 (2021)
Volume 12
Issue 7
According to clinical guidelines, the occurrence of very early-onset breast cancer (VEO-BC) (diagnosed ≤ age 30 years) or VEO ovarian cancer (VEO-OC) (diagnosed ≤ age 40 years) in families with BRCA1 or BRCA2 mutation (BRCAm) prompts advancing th
Autor:
Wei Liu, Ramzi Temanni, Puthen V. Jithesh, Remy Hobeika, Yvette Macary, Konduru S Sastry, Nancy Choucair, Monko Lek, Rashid Al-Ali, Aouatef Ismail Chouchane, Lotfi Chouchane, Ena Wang, Daniel G. MacArthur, Moncef M. Ladjimi, Francesco M. Marincola, Catherine M. Rose, Remy Thomas, André Mégarbané, Sara Tomei
Publikováno v:
BMC Medical Genetics
Background KCNH1 encodes a voltage-gated potassium channel that is predominantly expressed in the central nervous system. Mutations in this gene were recently found to be responsible for Temple-Baraitser Syndrome (TMBTS) and Zimmermann-Laband syndrom