Microdeletions and mutations of CREBBP (CBP) gene can cause
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Microdeletions and mutations of CREBBP (CBP) gene can cause
CBP truncating mutations in ovarian cancer
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
Microdeletions and mutations of CREBBP (CBP) gene can cause
Microdeletions and mutations of CREBBP (CBP) gene can cause
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients
Genes, Free Full-Text
CREB-binding Protein - an overview
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
CBP deficiency leads to HMT-mediated epigenetic modification. Induction
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
Rubinstein Syndrome - an overview
Genes, Free Full-Text
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