Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II
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| Description | scientific article published on 01 June 2012 |
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| Publication date | June 1, 2012 |
| Language | English |
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https://api.elsevier.com/content/article/PII:S1028455912000885?httpAccept=text/xml |
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| Missing/wrong data? | Edit Wikidata item |