[HTML][HTML] Identification of novel candidate genes and variants for hearing loss and temporal bone anomalies
RLP Santos-Cortez, TKL Yarza, TC Bootpetch… - Genes, 2021 - mdpi.com
Background: Hearing loss remains an important global health problem that is potentially
addressed through early identification of a genetic etiology, which helps to predict outcomes …
addressed through early identification of a genetic etiology, which helps to predict outcomes …
[HTML][HTML] Maxillofacial Changes in Melnick-Needles Syndrome
LL Albuquerque do Nascimento… - Case Reports in …, 2016 - hindawi.com
Background. Melnick-Needles Syndrome is rare congenital hereditary skeletal dysplasia
caused by mutations in the FLNA gene, which codifies the protein filamin A. This condition …
caused by mutations in the FLNA gene, which codifies the protein filamin A. This condition …