Varaico: Literature-Extracted Genetic Variants

Gene:FOXP1
Variant:p.M1insFs
Back to variants list

FOXP1

NM_001349338.3:p.M1insFs

Associated Papers

Childhood motor speech disorders: who to prioritise for genetic testing.

Van Niel H et al.

European Journal of Human Genetics : Ejhg, 2026

Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India.

Moirangthem A et al.

American Journal of Medical Genetics. Part A, 2021

Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa.

Thomford NE et al.

Omics : a Journal of Integrative Biology, 2018

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.

Bekheirnia MR et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."