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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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Case report: a Chinese girl like atypical Rubinstein–Taybi
Identification of the genetic basis of sporadic polydactyly in
Rubinstein‐Taybi syndrome in Chinese population with four novel
Established and emerging strategies to crack the genetic code of
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
IJMS, Free Full-Text
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Exon deletions of the EP300 and CREBBP genes in two children with
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