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rubinstein síndrome

Exon deletions of the EP300 and CREBBP genes in two children with

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Exon deletions of the EP300 and CREBBP genes in two children with
Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome
Exon deletions of the EP300 and CREBBP genes in two children with
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Exon deletions of the EP300 and CREBBP genes in two children with
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
Exon deletions of the EP300 and CREBBP genes in two children with
KMT2D acetylation by CREBBP reveals a cooperative functional interaction at enhancers in normal and malignant germinal center B cells
Exon deletions of the EP300 and CREBBP genes in two children with
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
Exon deletions of the EP300 and CREBBP genes in two children with
ZNF384-related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype
Exon deletions of the EP300 and CREBBP genes in two children with
Mutation spectrum of CREBBP and EP300 in RSTS individuals referenced in
Exon deletions of the EP300 and CREBBP genes in two children with
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Exon deletions of the EP300 and CREBBP genes in two children with
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch
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