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Q28485037-E9261971-F9D0-4B32-9FCA-7EC85D0D99F2
Q28485037-E9261971-F9D0-4B32-9FCA-7EC85D0D99F2
BestRank
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http://www.wikidata.org/entity/statement/Q28485037-E9261971-F9D0-4B32-9FCA-7EC85D0D99F2
Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome
P2860
Q28485037-E9261971-F9D0-4B32-9FCA-7EC85D0D99F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28485037-E9261971-F9D0-4B32-9FCA-7EC85D0D99F2
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Statement
wasDerivedFrom
89124c7f11bf2315bf91b094859145f1f0177c10
P2860
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis