| pubmed-article:984044 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:984044 | lifeskim:mentions | umls-concept:C0472801 | lld:lifeskim |
| pubmed-article:984044 | lifeskim:mentions | umls-concept:C1514721 | lld:lifeskim |
| pubmed-article:984044 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:984044 | pubmed:dateCreated | 1977-1-3 | lld:pubmed |
| pubmed-article:984044 | pubmed:abstractText | We have described the study of a small kindred with X-linked hemophilia A. It was ascertained through a clinically affected female, the daughter of a man with moderately severe hemophilia. The pedigree and the proband's phenotype suggest that she may be a heterozygote in whom most of the normal alleles at the VIII-1 locus are not active. She has two sisters, also obligatory carriers. The three sisters exhibit the three phenotypes possible for heterozygous females: clinically affected, clinically normal but phenotypically abnormal as determined by laboratory tests, and clinically and phenotypically normal. | lld:pubmed |
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| pubmed-article:984044 | pubmed:language | eng | lld:pubmed |
| pubmed-article:984044 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:984044 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:984044 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:984044 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:984044 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:984044 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:984044 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:984044 | pubmed:author | pubmed-author:MillerC HCH | lld:pubmed |
| pubmed-article:984044 | pubmed:author | pubmed-author:ReisnerH MHM | lld:pubmed |
| pubmed-article:984044 | pubmed:author | pubmed-author:ElstonR CRC | lld:pubmed |
| pubmed-article:984044 | pubmed:author | pubmed-author:GrahamJ BJB | lld:pubmed |
| pubmed-article:984044 | pubmed:author | pubmed-author:OliveJ AJA | lld:pubmed |
| pubmed-article:984044 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:984044 | pubmed:volume | 28 | lld:pubmed |
| pubmed-article:984044 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:984044 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:984044 | pubmed:pagination | 482-8 | lld:pubmed |
| pubmed-article:984044 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-H... | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-A... | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-H... | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-F... | lld:pubmed |
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| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-A... | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-F... | lld:pubmed |
| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-P... | lld:pubmed |
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| pubmed-article:984044 | pubmed:meshHeading | pubmed-meshheading:984044-G... | lld:pubmed |
| pubmed-article:984044 | pubmed:year | 1976 | lld:pubmed |
| pubmed-article:984044 | pubmed:articleTitle | The phenotypic range of hemophilia A carriers. | lld:pubmed |
| pubmed-article:984044 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:984044 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:984044 | pubmed:publicationType | Case Reports | lld:pubmed |
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