Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

VACTERL association, a relatively common condition with an incidence of approximately 1 in 20,000 – 35,000 births, is a non-random association of birth defects that includes vertebral defects (V), anal atresia (A), cardiac defects (C), tracheo-esophageal fistula (TE), renal anomalies (R) and limb ma...

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Hoofdauteurs: Agochukwu, Nneamaka B., Pineda-Alvarez, Daniel E., Keaton, Amelia A., Warren-Mora, Nicole, Raam, Manu S., Kamat, Aparna, Chandrasekharappa, Settara C., Solomon, Benjamin D.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2011
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3086932/
https://ncbi.nlm.nih.gov/pubmed/21315191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmg.2011.01.007
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