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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Rubinstein-Taybi syndrome in a Saudi boy with distinct features
PDF) New insights into genetic variant spectrum and genotype
IJMS, Free Full-Text
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Rubinstein‐Taybi syndrome in Chinese population with four novel
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Rubinstein‐Taybi syndrome in Chinese population with four novel
IJMS, Free Full-Text
Molecular Genetics & Genomic Medicine: Vol 7, No 12
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
Identification of the genetic basis of sporadic polydactyly in
Rubinstein–Taybi syndrome in diverse populations - Tekendo
High frequency of copy number imbalances in Rubinstein–Taybi
Genes, Free Full-Text
Exon deletions of the EP300 and CREBBP genes in two children with
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