Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability.

Autor: Kashevarova, Anna A.1 anna.kashevarova@medgenetics.ru, Nazarenko, Lyudmila P.2,3 ludmila.nazarenko@medgenetics.ru, Schultz-Pedersen, Soren4 docschultz@webspeed.dk, Skryabin, Nikolay A.1,5 nukulay@gmail.com, Salyukova, Olga A.2,3 olga.salukova@medgenetics.ru, Chechetkina, Nataliya N.2 valete@mail.ru, Tolmacheva, Ekaterina N.1 kate.tolmacheva@medgenetics.ru, Rudko, Aleksey A.6 aleksey.rudko@medgenetics.ru, Magini, Pamela7 pamela.magini@unibo.it, Graziano, Claudio7 claudio.graziano@unibo.it, Romeo, Giovanni7 giovanni.romeo@unibo.it, Joss, Shelagh8 Shelagh.Joss@ggc.scot.nhs.uk, Tümer, Zeynep9 asuman.zeynep.tuemer@regionh.dk, Lebedev, Igor N.1,3 igor.lebedev@medgenetics.ru
Zdroj: Molecular Cytogenetics (17558166). 2014, Vol. 7 Issue 1, p1-21. 21p.
Databáze: Academic Search Ultimate