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تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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DiGeorge embryology

DiGeorge embryology
Migration of neural crest cells during embryonic development and contribution to structures affected in DiGeorge syndrome with or without chromosome 22q11.2 deletion patients. The migration pathway of neural crest cells (orange) from the hindbrain to the brachial arch/pharyngeal pouch system and cardiac outflow tract is indicated by the arrows. Examples of affected malformations associated with perturbations in this developmental sequence are denoted.
AAA: aortic arch arteries; IAA: interrupted aortic arch; PDA: persistent ductus arteriosus.
Reproduced with permission from: Emanuel BS, et al. The genetic basis of conotruncal heart defects: The chromosome 22q11.2 deletion. In: Heart Development, Rosenthal N, Harvey R (Eds), Academic Press, 1998. Copyright © 1998 Elsevier.
Graphic 75948 Version 3.0

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