The laminopathies
Heterozygosity for a Mendelian disorder as a risk factor for complex disease
Predictive testing for Huntington disease
Developmental programming of hypothalamic feeding circuits
Stem cell research
Ironing out neurodegeneration
Characterizing genetic wrinkles in sperm of advanced paternal age
Genes for Joubert syndrome
Variability and inequity in testing of somatic tissue for hereditary cancer
Application of BRCA1 and BRCA2 mutation carrier prediction models in breast and/or ovarian cancer families of French Canadian descent
Hereditary lymphedema type I associated with VEGFR3 mutation
Germline mosaicism for a MECP2 mutation in a man with two Rett daughters
Dystrophic epidermolysis bullosa pruriginosa in Italy
Molecular background of polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome in a Polish population
Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients
A frameshift mutation in peroxisome-proliferator-activated receptor-γ in familial partial lipodystrophy subtype 3 (FPLD3; MIM 604367)