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

Rubinstein-Taybi syndrome Radiology Reference Article
Detecting Genetic Association of Common Human Facial Morphological

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with

Frontiers Integration of structural MRI and epigenetic analyses

Chemical and genetic rescue of an ep300 knockdown model for

PDF] Rubinstein-Taybi Syndrome Associated with Pituitary

Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome

PDF) Stress and the Emerging Roles of Chromatin Remodeling in

Genes, Free Full-Text

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

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

Rubinstein–Taybi syndrome in diverse populations - Tekendo
Two Pathogenic Variants in Two Ultra Rare Syndromes; Smith
de
por adulto (o preço varia de acordo com o tamanho do grupo)