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Q34329087-0CCDB196-A05E-404A-AF0B-D4A7AA1B4321
Q34329087-0CCDB196-A05E-404A-AF0B-D4A7AA1B4321
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http://www.wikidata.org/entity/statement/Q34329087-0CCDB196-A05E-404A-AF0B-D4A7AA1B4321
New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?
P2860
Q34329087-0CCDB196-A05E-404A-AF0B-D4A7AA1B4321
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34329087-0CCDB196-A05E-404A-AF0B-D4A7AA1B4321
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wasDerivedFrom
c3a14107a9c6cffa21babb0fa237663e3ac866f0
P2860
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)