DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Delahaye A, Khung-Savatovsky S, Aboura A. , et al.
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
Am J Med Genet A 2012;
158A (10) 2430-2438
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