Microdeletions and mutations of CREBBP (CBP) gene can cause
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A CRISPR Interference of CBP and p300 Selectively Induced Synthetic Lethality in Bladder Cancer Cells In Vitro
Microdeletions and mutations of CREBBP (CBP) gene can cause
CBP deficiency leads to HMT-mediated epigenetic modification. Induction
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH
Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients - Spena - 2015 - Clinical Genetics - Wiley Online Library
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability - Hussain - The Journal of Gene Medicine - Wiley Online Library
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
Microdeletions and mutations of CREBBP (CBP) gene can cause
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
CREB-binding protein - Wikipedia
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