Habibi, Laleh:


Retrotransposons and pediatric genetic disorders: Importance and implications

Gomes, Karina Braga:


Adiponectin gene polymorphisms: Association with childhood obesity

Caldwell, Kathleen S.;

Kreikemeier, Rose M.;

Lutz, Richard E.;

Esposito, Paul W.:


Osteogenesis imperfecta caused by

PPIB

mutation with severe phenotype and congenital hearing loss

Monti, Elena;

Venturi, Giacomo;

Gandini, Alberto;

Mottes, Monica;

Antoniazzi, Franco:


The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the

IFITM5

gene

Butler, Merlin G.:


Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome