ロード中...
Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis
We present the case of an 18-month-old boy with dysmorphic facial features, developmental delay, growth retardation, bilateral clubfeet, thrombocytopenia, and strabismus, whose array CGH analysis revealed concurrent de novo trisomy 10p11.22p15.3 and monosomy 7p22.3. We describe the patient's cl...
保存先:
| 主要な著者: | , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi Limited
2011-01-01
|
| シリーズ: | Case Reports in Genetics |
| オンライン・アクセス: | http://dx.doi.org/10.1155/2011/131768 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|