## Abstract The DiGeorge anomaly (DGA) is an etiologically heterogeneous developmental field defect in which cardiovascular malformations, hypocalcemia, thymic hypoplasia, and characteristic dysmorphisms are major clinical features. The 22q11.2 deletion is the most common single etiology of DGA, al
Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries
β Scribed by van Essen, Anthonie J. ;Schoots, Coen J. F. ;van Lingen, Richard A. ;Mourits, Marian J. E. ;Tuerlings, Joep H. A. M. ;Leegte, Bieke
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 371 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0148-7299
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