Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities - ScienceDirect
Por um escritor misterioso
Descrição
Frontiers Identifying and Predicting Autism Spectrum Disorder
Bi-allelic loss-of-function variants in TMEM147 cause moderate to
Cureus Rubinstein-Taybi Syndrome Associated with Pituitary
7,8-Dihydroxyflavone as a pro-neurotrophic treatment for
Clinical and mutational spectrum in Korean patients with
Anatomical and functional abnormalities on MRI in kabuki syndrome
PRRT2 mutation in a Japanese woman: Adult-onset focal epilepsy
Detecting Genetic Association of Common Human Facial Morphological
Dandy walker variant an association with Rubinstein Taybi syndrome
A novel de novo KCNB1 variant altering channel characteristics in
PRPS1 Mutations: Four Distinct Syndromes and Potential Treatment
PDF) 7,8-Dihydroxyflavone as a pro-neurotrophic treatment for
7,8-Dihydroxyflavone as a pro-neurotrophic treatment for
de
por adulto (o preço varia de acordo com o tamanho do grupo)
