Rubinstein-Taybi Syndrome 1
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The Rubinstein-Taybi Syndrome Children's Foundation
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Rubinstein-Taybi syndrome: MedlinePlus Genetics
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
Rubinstein - Taybi Syndrome (Rubinstein syndrome, broad thumb-hallux syndrome, broad thumbs and great toes, characteristic facies and mental retardation) - Dermatology Advisor
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
Rubinstein-Taybi Syndrome
History and Prevalence
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Severe persistent pulmonary hypertension in a neonate with Rubinstein–Taybi syndrome accompanied by triple X syndrome - Pediatrics & Neonatology
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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