DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms...

conditions such as frontonasal dysplasia, Waardenburg–Shah syndrome, and DiGeorge syndrome. Therefore, defining the mechanisms of neural crest development...

Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include...

uncontrollably. DiGeorge syndrome (known as 22q11.2 deletion) caused by a deletion in the 22nd chromosome. Some of the typical symptoms associated with DiGeorge Syndrome...

syndrome Turner syndrome Noonan syndrome Patau syndrome DiGeorge syndrome Cri du chat syndrome Edwards syndrome Fragile X syndrome Okamoto syndrome It...

The microprocessor complex subunit DGCR8 (DiGeorge syndrome critical region 8) is a protein that in humans is encoded by the DGCR8 gene. In other animals...

immunodeficiency now commonly referred to as DiGeorge syndrome. DiGeorge was the son of two Italian immigrants, Antonio DiGiorgio and his wife Emilia (née Taraborelli)...

Klinefelter's syndrome Ovaries in Fanconi anemia, gonadal dysgenesis, trisomy X Thymus in DiGeorge syndrome Labia majora in popliteal pterygium syndrome Corpus...

deletion syndromes are detectable using karyotyping techniques. DiGeorge syndrome or velocardiofacial syndrome – most common microdeletion syndrome Prader–Willi...

DNA-Ligase IV, common gamma chain, WHN-FOXN1, ZAP-70 and complete DiGeorge syndrome. It is fatal without treatment. The symptoms are very similar to graft-versus-host...