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Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate
BACKGROUND: 22q11.2 microdeletion syndrome is the most common multiple genetic disorder associated with learning disabilities, developmental delays, immune deficiency, hypocalcemia, and cleft palate. Finding some valid criteria for screening of 22q11.2 deletion syndromes in infants would be very hel...
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| 出版年: | Adv Biomed Res |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications & Media Pvt Ltd
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5220684/ https://ncbi.nlm.nih.gov/pubmed/28217639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.192728 |
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