Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2
- 12 May 2004
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 12 (8) , 604-612
- https://doi.org/10.1038/sj.ejhg.5201199
Abstract
No abstract availableKeywords
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