## Abstract A male patient with a de novo proximal interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3) is described with multiple anomalies and developmental delay. This patient's clinical manifestations are compared to previously reported patients with deletions of chro
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Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32))
โ Scribed by Mircher, Clotilde ;Rethore, Marie-Odile ;Lespinasse, James ;Fert-Ferrer, Sandra ;Lundsteen, Claes ;Kirchoff, Maria
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 86 KB
- Volume
- 118A
- Category
- Article
- ISSN
- 0148-7299
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