Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
Por um escritor misterioso
Last updated 03 abril 2025


A novel CREBBP mutation and its phenotype in a case of Rubinstein

KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Slow development causes, understanding global developmental delay

PDF) Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome

Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes

PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder

PDF) Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at

NIH creates Atlas of Human Malformation Syndromes in Diverse
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