## Abstract The first reported case of clinically significant congenital Factor VII deficiency in association with the 13q deletion syndrome is presented. It illustrates the importance of knowledge of the specific genes involved in gross deletion syndromes and adds to the current clinical experienc
13q deletion syndrome associated with retinoblastoma and clinical anophthalmos of the opposite eye
✍ Scribed by Hadjistilianou, Theodora ;Mastrangelo, Domenico ;Mazzotta, Cosimo ;Francesco, Sonia De ;Capretti, Cristina ;Lorè, Cosimo
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 53 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0098-1532
- DOI
- 10.1002/mpo.1332
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