Literature DB >> 15487011

Absence of deletion at the SOX2 locus in a case of microphthalmia and esophageal atresia.

Dominique Bonneau, Agnès Guichet, Françoise Boussion, Catherine Lépinard, Florence Biquard, Philippe Descamps.   

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Year:  2004        PMID： 15487011     DOI： 10.1002/ajmg.a.30180

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  1 in total

1.  Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia.

Authors:  Jie Zhou; Femida Kherani; Tanya M Bardakjian; James Katowitz; Nkecha Hughes; Lisa A Schimmenti; Adele Schneider; Terri L Young
Journal:  Mol Vis       Date:  2008-03-24       Impact factor: 2.367
  1 in total

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