| pubmed-article:2741940 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2741940 | lifeskim:mentions | umls-concept:C0005283 | lld:lifeskim |
| pubmed-article:2741940 | lifeskim:mentions | umls-concept:C0033053 | lld:lifeskim |
| pubmed-article:2741940 | lifeskim:mentions | umls-concept:C0080206 | lld:lifeskim |
| pubmed-article:2741940 | lifeskim:mentions | umls-concept:C1442164 | lld:lifeskim |
| pubmed-article:2741940 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:2741940 | pubmed:dateCreated | 1989-8-9 | lld:pubmed |
| pubmed-article:2741940 | pubmed:abstractText | During the course of prenatal diagnosis for beta-thalassemia in Chinese patients, we encountered a mutation that was not detectable by oligonucleotides for the known Chinese mutations. Amplification of the beta-globin gene by the polymerase chain reaction and direct DNA sequencing revealed a previously undescribed -30 TATA box mutation which was carried by the father. Prenatal diagnosis was achieved, and the fetus did not inherit this beta-thalassemia allele. | lld:pubmed |
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| pubmed-article:2741940 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2741940 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2741940 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2741940 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2741940 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2741940 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:2741940 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:2741940 | pubmed:author | pubmed-author:DohertyMM | lld:pubmed |
| pubmed-article:2741940 | pubmed:author | pubmed-author:KanY WYW | lld:pubmed |
| pubmed-article:2741940 | pubmed:author | pubmed-author:MokH YHY | lld:pubmed |
| pubmed-article:2741940 | pubmed:author | pubmed-author:ZhangJ ZJZ | lld:pubmed |
| pubmed-article:2741940 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2741940 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:2741940 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2741940 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2741940 | pubmed:pagination | 112-4 | lld:pubmed |
| pubmed-article:2741940 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:2741940 | pubmed:meshHeading | pubmed-meshheading:2741940-... | lld:pubmed |
| pubmed-article:2741940 | pubmed:year | 1989 | lld:pubmed |
| pubmed-article:2741940 | pubmed:articleTitle | A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia. | lld:pubmed |
| pubmed-article:2741940 | pubmed:affiliation | Department of Medicine, University of California, San Francisco 94143-0724. | lld:pubmed |
| pubmed-article:2741940 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2741940 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:2741940 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2741940 | lld:pubmed |
