Chromosome 22q11.2 deletion causes Di-George syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome with tetralogy of Fallot (TOF), and sporadic or familial TOF. To determine the prevalence and clinical importance of the 22q 11.2 deletion in TOF, a series of 212 Japanese TOF patients
β¦ LIBER β¦
Tetralogy of fallot with pulmonary atresia associated with chromosome 22q11 deletion
β Scribed by Kazuo Momma; Chisato Kondo; Rumiko Matsuoka
- Book ID
- 119170937
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 655 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1558-3597
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