Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes
Por um escritor misterioso
Descrição
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
Human genetics and molecular genomics of Chiari malformation type 1: Trends in Molecular Medicine
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Rubinstein-Taybi Syndrome 1
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
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 in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
PDF) Exogenous and endogenous HDAC inhibitor effects in Rubinstein-Taybi syndrome models
Smith's Recognizable Patterns of Human Malformation - 8th Edition
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience
de
por adulto (o preço varia de acordo com o tamanho do grupo)
