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Object |
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Journal Article|Research Support, Non-U.S. Gov't|Research Support, U.S. Gov't, P.H.S. |
| endingPage |
134 |
| issn |
0964-6906
1460-2083 |
| issueIdentifier |
1 |
| pageRange |
129-134 |
| publicationName |
Human Molecular Genetics |
| startingPage |
129 |
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| bibliographicCitation |
Decker RA, Peacock ML, Watson P. Hirschsprung Disease in MEN 2A: Increased Spectrum of RET Exon 10 Genotypes and Strong Genotype--Phenotype Correlation. Human Molecular Genetics. 1998 Jan 01;7(1):129–34. doi: 10.1093/hmg/7.1.129. |
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| date |
1998-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1093/hmg/7.1.129
https://pubmed.ncbi.nlm.nih.gov/9384613 |
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https://portal.issn.org/resource/ISSN/0964-6906
https://portal.issn.org/resource/ISSN/1460-2083 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Hirschsprung Disease in MEN 2A: Increased Spectrum of RET Exon 10 Genotypes and Strong Genotype--Phenotype Correlation |
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