Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts theHOXD gene cluster
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference34 articles.
1. Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families
2. Mild mandibulofacial dysostosis in a child with a deletion of 3p
3. Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B
4. Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis
5. Monodactylous Limbs and Abnormal Genitalia Are Associated with Hemizygosity for the Human 2q31 Region That Includes the HOXD Cluster
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