Author's response to reviews Title: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results Authors:
نویسندگان
چکیده
”Conclusions In this study, the use of an ultra high-resolution SNP array did not contribute to further diagnosis of developmental disorders of unknown cause. The statistical power of these results is limited by the small size of the patient cohort, and interpretation of these negative results can only be applied to the patients studied here.” Page 11: ”Also, it is important to note that the statistical power is limited by the small size of our patient cohort, and thus results are not entirely comparable with Bernardini and Mannik’s.”
منابع مشابه
کاربردهای فن دو رگه‌سازی ژنومی مقایسه‌ای آرایه در سرطان و بیماری‌های ژنتیکی: مقاله مروری
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متن کاملAuthor's response to reviews Title: The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome Authors:
متن کامل
P-243: Prenatal Diagnosis Using Array CGH: Case Presentation
Background: Karyotype analysis has been the standard and reliable procedure for prenatal cytogenetic diagnosis since the 1970s. However, the major limitation remains requirement for cell culture, resulting in a delay of as much as 14 days to get the test results.CGH array technology has proven to be useful in detecting causative genomic imbalances or genetic mutations in as many as 15% of child...
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تاریخ انتشار 2011