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The genetics of osteoporosis: 'complexities and difficulties'
Rett syndrome: The influence of dysregulated gene slicing
Involvement of an inflammation-related gene in X-linked mental retardation
Breaking the law: the molecular basis of non-Mendelian transmission
Xolótl: god of monstrosities
Comparison of the role of dopamine, serotonin, and noradrenaline genes in ADHD, ODD and conduct disorder: multivariate regression analysis of 20 genes
A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations
A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor
A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes
Molecular analysis of the 5′-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemia
Spina bifida and common mutations at the homocysteine metabolism pathway
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation
Identification of cystic fibrosis mutations in Oman