World Society of Child Science

Volume 3, Number 1, Year 2014

Review Articles
Usha R. Dutta
Precision in chromosome identification with leads in molecular cytogenetics: An illustrated review

• Abstract
• PDF 169 KB

Seyed M. Akrami and Laleh Habibi
Retrotransposons and pediatric genetic disorders: Importance and implications

• Abstract
• PDF 281 KB

Original Article
Vanêssa Gomes Fraga and Karina Braga Gomes
Adiponectin gene polymorphisms: Association with childhood obesity

• Abstract
• PDF 431 KB

Case Reports
Eric T. Rush, Kathleen S. Caldwell, Rose M. Kreikemeier, Richard E. Lutz, and Paul W. Esposito
Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and congenital hearing loss

• Abstract
• PDF 348 KB

Massimiliano Corradi, Elena Monti, Giacomo Venturi, Alberto Gandini, Monica Mottes, and Franco Antoniazzi
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene

• Abstract
• PDF 186 KB

Adria M. Jerkovich and Merlin G. Butler
Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome

• Abstract
• PDF 48 KB