Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
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Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Genes, Free Full-Text
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
PDF) Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome
Rubinstein-Taybi Syndrome: Presentation in the First Month of Life - The Journal of Pediatrics
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
PDF) Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly
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