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Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in the LDLR gene.
J Appl Genet. 2008;49(1):109-13. doi: 10.1007/BF03195256.
J Appl Genet. 2008.
PMID: 18263977
Further delineation of the classical Smith-Lemli-Opitz syndrome phenotype at different patient ages: clinical and biochemical studies.
Krajewska-Walasek M, Gradowska W, Ryzko J, Socha P, Chmielik J, Szapłyko W, Kasprzyk J, Górska B, Szreter M, Wolski J, Rysiewski H, Małunowicz EM, Gregorek H, Michałkiewicz J, Pietraszek E, Szapłyko J.
Krajewska-Walasek M, et al. Among authors: szaplyko j.
Clin Dysmorphol. 1999 Jan;8(1):29-40.
Clin Dysmorphol. 1999.
PMID: 10327249
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