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A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
Nat Genet. 1998 Dec;20(4):358-61. doi: 10.1038/3828.
Nat Genet. 1998.
PMID: 9843207
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.
Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, Nixon P, Papapetrou C, Winter RM, Edwards Y, Morrison K, Barrow M, Cordier-Alex MP, Correia P, Galvin-Parton PA, Gaskill S, Gaskin KJ, Garcia-Minaur S, Gereige R, Hayward R, Homfray T.
Hagan DM, et al. Among authors: custard e.
Am J Hum Genet. 2000 May;66(5):1504-15. doi: 10.1086/302899. Epub 2000 Apr 4.
Am J Hum Genet. 2000.
PMID: 10749657
Free PMC article.
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Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.
Lemonde HA, Custard EJ, Bouquet J, Duran M, Overmars H, Scambler PJ, Clayton PT.
Lemonde HA, et al. Among authors: custard ej.
Gut. 2003 Oct;52(10):1494-9. doi: 10.1136/gut.52.10.1494.
Gut. 2003.
PMID: 12970144
Free PMC article.
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Analysis of factor VIII mediated suppression of lentiviral vector titres.
Radcliffe PA, Sion CJ, Wilkes FJ, Custard EJ, Beard GL, Kingsman SM, Mitrophanous KA.
Radcliffe PA, et al. Among authors: custard ej.
Gene Ther. 2008 Feb;15(4):289-97. doi: 10.1038/sj.gt.3303080. Epub 2007 Nov 29.
Gene Ther. 2008.
PMID: 18046428
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