New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

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New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
PDF) New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐ positive patients
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
The role of KAT3 proteins in neural development
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Divergent variant patterns among 19 patients with Rubinstein‐Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing - Enomoto - 2022 - Clinical Genetics - Wiley Online Library
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Genes, Free Full-Text
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
PDF) Intragenic duplication of EHMT1 gene results in Kleefstra syndrome
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
PDF) New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐ positive patients
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome - Choi - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Genes, Free Full-Text
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Examples of exon array comparative genomic hybridization data from four
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
New insights into genetic variant spectrum and genotype–phenotype  correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients -  Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley  Online Library
PDF) Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly
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