Síndrome de Rubinstein-Taybi

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

SciELO - Brasil - Broad thumbs and broad hallux: the hallmarks for the Rubinstein-Taybi syndrome Broad thumbs and broad hallux: the hallmarks for the Rubinstein-Taybi syndrome

Minha história: Christiane, Isabela e a síndrome de Rubinstein-Taybi - Portal Acesse

Facial features of Rubinstein-Taybi syndrome

Genes, Free Full-Text

sindrome rara rubinstein-taybi Estella

DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs

SÍNDROME DE RUBINSTEIN-TAYBI - CANAL INFANTIL