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
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Rubinstein–Taybi syndrome: clinical and molecular overview
Molecular analysis of the CBP gene in 60 patients with Rubinstein
Rubinstein-Taybi syndrome with scoliosis treated with single-stage
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Rubinstein–Taybi syndrome in diverse populations - Tekendo
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
Duplications of the critical Rubinstein–Taybi deletion region on
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
High frequency of copy number imbalances in Rubinstein–Taybi
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein–Taybi syndrome - Wikipedia
Clinical, genetic and imaging findings identify new causes for
PDF) Clinical, genetic and imaging findings identify new causes
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