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Q36216971-8A9F9BC0-0194-4550-B4B5-E3552665EC6F
Q36216971-8A9F9BC0-0194-4550-B4B5-E3552665EC6F
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Statement
http://www.wikidata.org/entity/statement/Q36216971-8A9F9BC0-0194-4550-B4B5-E3552665EC6F
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes
P2860
Q36216971-8A9F9BC0-0194-4550-B4B5-E3552665EC6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36216971-8A9F9BC0-0194-4550-B4B5-E3552665EC6F
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wasDerivedFrom
7a3e2da1d8c6da52b87b7684b653e400783fa757
P2860
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis