pubmed-article:3833909 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C0000769 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C0015914 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C2718310 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C0010802 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C0185125 | lld:lifeskim |
pubmed-article:3833909 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:3833909 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:3833909 | pubmed:dateCreated | 1986-5-30 | lld:pubmed |
pubmed-article:3833909 | pubmed:abstractText | A study of 100 sperm karyotypes from 8 normal subjects was carried out using the technique of in vitro hetero-specific human-hamster fertilisation. 19 of those showed some abnormality. 17% of those were hyperploidies or hypoploidies and 2% showed structural abnormalities. A study carried out at the same time on 34 hamster egg karyotypes showed 6 hypoploidies and 1 hyperploidy. In effect oa cytogenetic technique which is very similar to this one makes it possible to analyse the human oocyte karyotype. The results found in these samples of motile sperms show a higher incidence of abnormality than in other published series, but these figures can not be extrapolated to the composition of in vivo whole sperms. | lld:pubmed |
pubmed-article:3833909 | pubmed:language | fre | lld:pubmed |
pubmed-article:3833909 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3833909 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:3833909 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3833909 | pubmed:issn | 0368-2315 | lld:pubmed |
pubmed-article:3833909 | pubmed:author | pubmed-author:SeleBB | lld:pubmed |
pubmed-article:3833909 | pubmed:author | pubmed-author:PellestorFF | lld:pubmed |
pubmed-article:3833909 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3833909 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:3833909 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3833909 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3833909 | pubmed:pagination | 997-1003 | lld:pubmed |
pubmed-article:3833909 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:3833909 | pubmed:meshHeading | pubmed-meshheading:3833909-... | lld:pubmed |
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pubmed-article:3833909 | pubmed:year | 1985 | lld:pubmed |
pubmed-article:3833909 | pubmed:articleTitle | [Cytogenetics of human gametes: its application to the study of fertilization anomalies]. | lld:pubmed |
pubmed-article:3833909 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3833909 | pubmed:publicationType | English Abstract | lld:pubmed |
pubmed-article:3833909 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:3833909 | lld:pubmed |