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Short arm deletion of chromosome 1: del(1)(p13.3 p22.3) in a female infant with an extreme tetralogy of Fallot

โœ Scribed by Hiroshi Tabata; Katsuhiko Sone; Toshihiro Kobayashi; Takayuki Yanagisawa; Tadahisa Tamura; Nobuzou Shimizu; Yuzuru Kanbe; Masahiko Tashiro; Sanayasu Ono; Takayoshi Kuroume


Book ID
115090155
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
266 KB
Volume
39
Category
Article
ISSN
0009-9163

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Interstitial deletion of the short arm o
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## 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