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European Journal of Human Genetics : EJHG|July 18, 2013
An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3Céline Pebrel-Richard, Anne Debost-Legrand, Eléonore Eymard-Pierre, et al.Journal of Advanced Nursing|May 20, 2023
Clinical practice recommendations for nurse-administered intramuscular injections in mental health: A modified Delphi studyCandy Guiguet-Auclair, Lise Bernard, Stéphane Boisgard, et al.Pageof 4