22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features
Introduction: Deletion 22q11.2 occurs in 1:4,000-1:6,000 live births while 10p13p14 deletion is found in 1:200,000 newborns. Both deletions have similar clinical features such as congenital heart disease and immunological anomalies.Objective: We looked for a 22q11.2 deletion in Mexican patients wi...
में बचाया:
| में प्रकाशित: | Colombia Médica |
|---|---|
| मुख्य लेखकों: | , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Universidad del Valle
2018
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| विषय: | |
| ऑनलाइन पहुंच: | https://www.redalyc.org/articulo.oa?id=28357492005 https://www.redalyc.org/journal/283/28357492005/ https://www.redalyc.org/journal/283/28357492005/html/ https://www.redalyc.org/journal/283/28357492005/28357492005.epub https://www.redalyc.org/journal/283/28357492005/movil |
| टैग: |
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