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
Exclusion of 22qll deletion in noonan syndrome with tetralogy of fallot
β Scribed by Digilio, Maria Cristina ;Marino, Bruno ;Giannotti, Aldo ;Dallapiccola, Bruno
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 156 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0148-7299
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