Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1–p21.3
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference31 articles.
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2. The mapping of a gene for craniosynostosis: Evidence for linkage of the Saethre—Chotzen syndrome to distal chromosome 7p;Brueton;J. Med. Genet.,1992
3. A comprehensive classification of homeobox genes;Bürglin,1994
4. Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos;Candia;Development,1992
5. Amino acid sequence of Mox-2 and comparison to its Xenopus and rat homologues;Candia;Nucleic Acids Res.,1993
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