Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies
Resource Type
Authors
Chiara Legnaro ; Maria Leine Guion-Almeida ; Antonio Richieri-Costa ; Lucilene Arilho Ribeiro-Bicudo ; Rodrigo Gonçalves Quiezi
Source
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual) Universidade de São Paulo (USP) instacron:USP
Subject
SÍNDROMES OROFACIODIGITAIS Adolescent Craniofacial Abnormalities Dysgenesis Genetics Medicine Humans In patient Abnormalities, Multiple Eye Abnormalities Callosal agenesis Child Gene Genetics (clinical) Encephalocele Homeodomain Proteins business.industry Infant Anatomy Syndrome DNA-Binding Proteins Repressor Proteins Child, Preschool Face Mutation Female Basal encephalocele Agenesis of Corpus Callosum business Transcription Factors
Language
ISSN
1552-4833