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Q42290485-E80BEED1-E525-44D5-80F8-5289CBE8808C
Q42290485-E80BEED1-E525-44D5-80F8-5289CBE8808C
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http://www.wikidata.org/entity/statement/Q42290485-E80BEED1-E525-44D5-80F8-5289CBE8808C
Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype.
P2860
Q42290485-E80BEED1-E525-44D5-80F8-5289CBE8808C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42290485-E80BEED1-E525-44D5-80F8-5289CBE8808C
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wasDerivedFrom
8ddb392a6e3d496b008e6692e1cd88428d742812
P2860
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.