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t/gene-pbx1

PBX1 gene

Discuss publications and research concerning the PBX1 gene.

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Related literature

Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis.
PBX1
[Clinical phenotype and genetic analysis of a child with CAKUTHED syndrome due to variant of PBX1 gene].
PBX1
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal Death.
PBX1
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children.
PBX1
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
PBX1
Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.
PBX1
Prognostic significance of FLT3 mutational status and expression levels in MLL-AF4+ and MLL-germline acute lymphoblastic leukemia.
PBX1
Antigen expression patterns reflecting genotype of acute leukemias.
PBX1

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