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Object |
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| endingPage |
902 |
| issn |
1018-4813
1476-5438 |
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8 |
| pageRange |
897-902 |
| publicationName |
European journal of human genetics : EJHG |
| startingPage |
897 |
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| bibliographicCitation |
Neerman-Arbez M, Antonarakis SE, Honsberger A, Morris MA. The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster. European Journal of Human Genetics. 1999 Dec 08;7(8):897–902. doi: 10.1038/sj.ejhg.5200395. |
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| date |
1999-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1038/sj.ejhg.5200395
https://pubmed.ncbi.nlm.nih.gov/10602365 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/8515
https://portal.issn.org/resource/ISSN/1018-4813 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://scigraph.springernature.com/
https://www.crossref.org/ |
| title |
The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster |
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http://id.nlm.nih.gov/mesh/M0008430 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10737
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_f9d769af0e91c5ceee335c68e627425d
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8937 |