reference/10690659

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bibliographicCitation	Delahaye A, Khung‐Savatovsky S, Aboura A, Guimiot F, Drunat S, Alessandri J, Gérard M, Bitoun P, Boumendil J, Robin S, Huel C, Guilherme R, Serero S, Gressens P, Elion J, Verloes A, Benzacken B, Delezoide A, Pipiras E. Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. American J of Med Genetics Pt A. 2012 Aug 17;158A(10):2430–8. doi: 10.1002/ajmg.a.35548.
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date	2012-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.a.35548 https://pubmed.ncbi.nlm.nih.gov/22903608
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene
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