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 diverse populations - Tekendo
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Clinical exome sequencing identifies novel CREBBP variants in 18
Identification of the genetic basis of sporadic polydactyly in
New insights into genetic variant spectrum and genotype–phenotype
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Case report: a Chinese girl like atypical Rubinstein–Taybi
Clinical exome sequencing identifies novel CREBBP variants in 18
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
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