Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review

• Main Authors: Gabriele Tonni (Author), Marcella Palmisano (Author), Ana Cristina Perez Zamarian (Author), Ana Carolina Rabachini Caetano (Author), Eduardo Félix Martins Santana (Author), Alberto Borges Peixoto (Author), Edecio Armbruster-Moraes (Author), Rodrigo Ruano (Author), Edward Araujo Júnior (Author)
• Format: Book
• Published: Elsevier, 2019-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

The aim of the current review is to report a-CGH abnormalities identified in fetuses with prenatally diagnosed fetal malformations in whom a normal karyotype was diagnosed with conventional cytogenetic analysis.A systematic electronic search of databases (PubMed/Medline, EMBASE/SCOPUS) has been cond...