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Q52138436-FFAC9004-B686-4622-8545-405EEAE98CEC
Q52138436-FFAC9004-B686-4622-8545-405EEAE98CEC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52138436-FFAC9004-B686-4622-8545-405EEAE98CEC
Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof-of-concept examples.
P2860
Q52138436-FFAC9004-B686-4622-8545-405EEAE98CEC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52138436-FFAC9004-B686-4622-8545-405EEAE98CEC
rank
NormalRank
type
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Statement
wasDerivedFrom
d7902bfefe17e2c9cdb6ebf2ce2d55a4f51e7b11
P2860
TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype