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. (Q47618208)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
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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. (English)
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Charles H C M Buys
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Grzegorz M Burzynski
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Ilja M Nolte
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Jan Osinga
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Bas Twigt
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Saskia Maas
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Alice Brooks
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Joke Verheij
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Ivan Plaza Menacho
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1 August 2004
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12
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8
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604-612
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