We report on a patient with DiGeorge syndrome (DGS) phenotype or anomaly and an unbalanced translocation [45,XY,-10,-22, +der(10),t(10;22)(p13;q11)] resulting in monosomy of 10p13-pter and 22q11-pter. Because both regions involved in this rearrangement have been implicated in DGS, we performed a mol
No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585
โ Scribed by Bartsch, Oliver; Wagner, Annett; Hinkel, Georg Klaus; Lichtner, Peter; Murken, Jan; Schuffenhauer, Simone
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 13 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19990423)83:5<425::aid-ajmg17>3.0.co;2-q
No coin nor oath required. For personal study only.
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