Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Surgical treatment of scoliosis in Rubinstein-Taybi syndrome type 2: a case report – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science
High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Genes, Free Full-Text
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
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
PDF) Rubinstein-Taybi syndrome medical guidelines
PDF) Rubinstein-Taybi syndrome medical guidelines
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