Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities - ScienceDirect
Por um escritor misterioso
Descrição

Frontiers Integration of structural MRI and epigenetic analyses

Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel

PDF) Application of chromosome microarray analysis in patients

7,8-Dihydroxyflavone as a pro-neurotrophic treatment for

Frameshift Mutation in Polar Rich Domain (PRD) of PQBP1 Gene

Bi-allelic loss-of-function variants in TMEM147 cause moderate to

Rubinstein–Taybi syndrome associated with Chiari type I

PDF) 7,8-Dihydroxyflavone as a pro-neurotrophic treatment for

Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome

Chemical and genetic rescue of an ep300 knockdown model for
de
por adulto (o preço varia de acordo com o tamanho do grupo)