Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC)

Author:

Bergmann Carsten,Zerres Klaus,Peschgens Thomas,Senderek Jan,Hörnchen Helmut,Rudnik-Schöneborn Sabine

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. The contribution of the adriamycin-induced rat model of the VATER association to our understanding of congenital abnormalities and their embryogenesis;Beasley;Pediatr Surg Int,2000

2. Polytopic anomalies with agenesis of the lower vertebral column;Bohring;Am J Med Genet,1999

3. Retinoic acid embryopathy: Case report and review of literature;Coberly;Pediatr Pathol Lab Med,1996

4. VACTERL with the mitochondrial np 3243 point mutation;Damian;Am J Med Genet,1996

5. Severe axial mesodermal dysplasia spectrum in an infant of a diabetic mother;Depraetere;Genet Couns,1995

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