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Article

[Clinical phenotype of a patient with FOXP1 deletion].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Apr 2015

Blanco Sánchez T, Duat Rodríguez A, Cantarín Extremera V, Lapunzina P, Palomares Bralo M, Nevado Blanco J

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Share to Developmental Disabilities
Share to Child, Preschool
Share to Forkhead Transcription Factors
Share to Gene Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to FOXP1 gene

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Source

Identifiers

PMID: 25037997
DOI: 10.1016/j.anpedi.2014.06.007

Genes

FOXP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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