SciELO - Brasil - Síndrome de Rubinstein-Taybi: anomalias físicas, manifestações clínicas e avaliação auditiva Síndrome de Rubinstein-Taybi: anomalias físicas, manifestações clínicas e avaliação auditiva
IJMS | Free Full-Text | Whole Exome Sequencing for a Patient with Rubinstein -Taybi Syndrome Reveals de Novo Variants besides an Overt CREBBP Mutation
Síndrome de Rubinstein-Taybi, atención odontoestomatológica a pacientes especiales: reporte de caso clínico
Hedgehog signaling update - Cohen Jr. - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
A, Patient 13 at the age of 23 years. Note sloping forehead,... | Download Scientific Diagram
Síndrome de Rubinstein-Taybi
SciELO - Brasil - Anestesia em paciente com síndrome de Rubinstein-Taybi: relato de caso Anestesia em paciente com síndrome de Rubinstein-Taybi: relato de caso
Face scanning and spontaneous emotion preference in Cornelia de Lange syndrome and Rubinstein-Taybi syndrome | Journal of Neurodevelopmental Disorders | Full Text
Síndrome de Rubinstein-Taybi: Causas, características y tratamiento - CSC
Síndrome de Rubinstein-Taybi
Rubinstein taybi presentation | PPT
Síndrome de Rubinstein-Taybi, atención odontoestomatológica a pacientes especiales: reporte de caso clínico
Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers - Wieczorek - 2009 - American Journal of Medical Genetics Part A -
Genes | Free Full-Text | Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes | European Journal of Human Genetics
Síndrome de Rubinstein-Taybi - Wikipedia, la enciclopedia libre
Síndrome de Rubinstein Taybi: características fenotípicas, reporte de caso.
Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers - Wieczorek - 2009 - American Journal of Medical Genetics Part A -
Síndrome de Rubinstein Taybi: características fenotípicas, reporte de caso.
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Divergent variant patterns among 19 patients with Rubinstein‐Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing - Enomoto - 2022 - Clinical Genetics - Wiley Online Library
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant | BMC Medical Genetics | Full Text
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes | European Journal of Human Genetics
Síndrome de Rubinstein-Taybi asociado a hipoplasia de una extremidad. Comunicación de un caso neonatal
