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Q48267975-41F710C7-6820-43B0-AC24-4FC5A5DE4911
Q48267975-41F710C7-6820-43B0-AC24-4FC5A5DE4911
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http://www.wikidata.org/entity/statement/Q48267975-41F710C7-6820-43B0-AC24-4FC5A5DE4911
SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements.
P2860
Q48267975-41F710C7-6820-43B0-AC24-4FC5A5DE4911
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48267975-41F710C7-6820-43B0-AC24-4FC5A5DE4911
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wasDerivedFrom
fa320add992f28b354e524ac198c4e987e9b6b32
P2860
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.