Genome-wide sequencing for unexplained developmental delays and multiple congenital anomalies a rapid qualitative review
About one half of people living with congenital anomalies have not had a specific cause or diagnosis identified based on their clinical presentation or examination of environmental causes. Such individuals are given a label of "unexplained developmental delay", and it is not uncommon for t...
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| Format: | eBook |
| Language: | English |
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Ottawa
CADTH
May 16, 2019, 2019
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| Edition: | Version 1.0 |
| Series: | CADTH rapid response report: summary with critical appraisal
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| Collection: | National Center for Biotechnology Information - Collection details see MPG.ReNa |
Table of Contents:
- Includes bibliographical references