A clinical study of 31 individuals with midline facial defects with hypertelorism and a guideline for follow-up

Arquivos de Neuro-Psiquiatria

Volumn 65, Issue 2 B, 2007, Pages 396-401

  Gil da Silva Lopes, Vera Lúcia ^a   Maciel Guerra, Andréa Trevas ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

Craniofacial anomalies; Facial clefts; Follow up; Frontonasal dysplasia; Frontonasal process; Ocular hypertelorism

Indexed keywords

ADULT; ARTICLE; CENTRAL NERVOUS SYSTEM DISEASE; CLINICAL ARTICLE; CLINICAL EXAMINATION; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; EYE DISEASE; FACE MALFORMATION; FEMALE; FOLLOW UP; GENETIC ANALYSIS; HUMAN; HYPERTELORISM; INFANT; MALE; PRACTICE GUIDELINE; PRESCHOOL CHILD; SCHOOL CHILD; SKULL DEFECT;

EID: 34547623540     PISSN: 0004282X     EISSN: 16784227     Source Type: Journal    
DOI: 10.1590/S0004-282X2007000300006     Document Type: Article

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