## Abstract Haploinsufficiency of chromosome 22q11.2 is a wellβestablished cause of both the DiGeorge anomaly and the velocardiofacial syndrome. This condition shows a continuous spectrum of phenotypic manifestations with a considerable interβ and intrafamilial variability. We report on a threeβgen
β¦ LIBER β¦
Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion
β Scribed by J-S Fang; K-F Lee; C-T Huang; C-L Syu; K-J Yang; L-H Wang; D-L Liao; C-H Chen
- Book ID
- 110888596
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 408 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0009-9163
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