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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50
has manifestation of work	http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50/issue_12/m/print http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50/issue_12/m/web
Date Copyrighted	2013
Rights	Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
issue	12
is Is Part Of of	Genetic variants in CHI3L1 influencing YKL-40 levels: resequencing 900 individuals and genotyping 9000 individuals from the general population A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial network Criteria and prediction models for mismatch repair gene mutations: a review A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men Association analyses identifying two common susceptibility loci shared by psoriasis and systemic lupus erythematosus in the Chinese Han population

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