Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference2 articles.
1. Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery;von Gernet;Clin Genet,2000
2. Contribution of tridimensional sonography and magnetic resonance imaging to prenatal diagnosis of Apert syndrome at mid-trimester;Boog;Fetal Diagn Ther,1999
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