| pubmed-article:5697353 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0039730 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0019016 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0062278 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0205197 | lld:lifeskim |
| pubmed-article:5697353 | lifeskim:mentions | umls-concept:C0301625 | lld:lifeskim |
| pubmed-article:5697353 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:5697353 | pubmed:dateCreated | 1969-1-8 | lld:pubmed |
| pubmed-article:5697353 | pubmed:abstractText | A family study is reported in which all three siblings were shown to be doubly heterozygous for haemoglobin D Los Angeles and beta thalassaemia, which resulted in a complete suppression of haemoglobin A synthesis. This demonstrates the effects of genetic interaction which occur when the genes for haemoglobin D Los Angeles and beta thalassaemia are both transmitted to the offspring. The importance of family studies in the investigation of haemoglobin abnormalities is stressed. | lld:pubmed |
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| pubmed-article:5697353 | pubmed:language | eng | lld:pubmed |
| pubmed-article:5697353 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5697353 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:5697353 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:5697353 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:5697353 | pubmed:issn | 0021-9746 | lld:pubmed |
| pubmed-article:5697353 | pubmed:author | pubmed-author:Marengo-RoweA... | lld:pubmed |
| pubmed-article:5697353 | pubmed:author | pubmed-author:McCrackenA... | lld:pubmed |
| pubmed-article:5697353 | pubmed:author | pubmed-author:FlanaganPP | lld:pubmed |
| pubmed-article:5697353 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:5697353 | pubmed:volume | 21 | lld:pubmed |
| pubmed-article:5697353 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:5697353 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:5697353 | pubmed:pagination | 508-10 | lld:pubmed |
| pubmed-article:5697353 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:5697353 | pubmed:year | 1968 | lld:pubmed |
| pubmed-article:5697353 | pubmed:articleTitle | Complete suppression of haemoglobin A synthesis in haemoglobin D Los Angeles--beta thalassaemia. | lld:pubmed |
| pubmed-article:5697353 | pubmed:publicationType | Journal Article | lld:pubmed |
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