Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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PDF) Identification of the genetic basis of sporadic polydactyly
Identification of the genetic basis of sporadic polydactyly in
Rubinstein‐Taybi syndrome in Chinese population with four novel
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Genes, Free Full-Text
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Further delineation of an entity caused by CREBBP and EP300
PDF) New insights into genetic variant spectrum and genotype
Clinical exome sequencing identifies novel CREBBP variants in 18
Case report: a Chinese girl like atypical Rubinstein–Taybi
PDF) Identification of the genetic basis of sporadic polydactyly
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