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| pubmed-article:9326924 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:9326924 | pubmed:dateCreated | 1997-11-14 | lld:pubmed |
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| pubmed-article:9326924 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9326924 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:9326924 | pubmed:issn | 1061-4036 | lld:pubmed |
| pubmed-article:9326924 | pubmed:author | pubmed-author:KolodnerRR | lld:pubmed |
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| pubmed-article:9326924 | pubmed:author | pubmed-author:Osei-MensaSS | lld:pubmed |
| pubmed-article:9326924 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9326924 | pubmed:volume | 17 | lld:pubmed |
| pubmed-article:9326924 | pubmed:owner | NLM | lld:pubmed |
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| pubmed-article:9326924 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9326924 | pubmed:articleTitle | A human compound heterozygote for two MLH1 missense mutations. | lld:pubmed |
| pubmed-article:9326924 | pubmed:publicationType | Letter | lld:pubmed |
| pubmed-article:9326924 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9326924 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:9326924 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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