Rubinstein–Taybi syndrome European Journal of Human Genetics

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Last updated 20 março 2025
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Rubinstein–Taybi syndrome  European Journal of Human Genetics
EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients - Cohen - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Psychiatric Profile in Rubinstein-Taybi Syndrome
Rubinstein–Taybi syndrome  European Journal of Human Genetics
New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Rubinstein–Taybi syndrome  European Journal of Human Genetics
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Rubinstein-Taybi Syndrome
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Genes, Free Full-Text
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Forgotten Diseases Research Foundation
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Genes, Free Full-Text
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children - Du - 2023 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Rubinstein-Taybi syndrome. Journal of Medical Genetics
Rubinstein–Taybi syndrome  European Journal of Human Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein–Taybi syndrome  European Journal of Human Genetics
PDF) Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
Rubinstein–Taybi syndrome  European Journal of Human Genetics
EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients - Cohen - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

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