Zobrazeno 1 - 4
of 4
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
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:
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
Autor:
Imbert-Bouteille, Marion, Corsini, Carole, Picot, Marie-Christine, Mizrahy, Lucas, Akouete, Sandrine, Huguet, Helena, Thomas, Frédéric, Geneviève, David, Taourel, Patrice, Ychou, Marc, Galibert, Virginie, Rideau, Chloé, Baudry, Karen, Kogut Kubiak, Tatiana, Coupier, Isabelle, Hobeika, Rémy, Macary, Yvette, Toledano, Alain, Solassol, Jérôme, Maalouf, Antoine
Publikováno v:
Genes; Jul2021, Vol. 12 Issue 7, p1100, 1p