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Identification of clinically significant%2C submicroscopic c…
Identification of clinically significant%2C submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.
Identification of clinically significant%2C submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.
Article, Chapter
Authors: B.H.W. Faas
Publication: Journal of Medical Genetics, Volume:47, Issue:9, Page(s):586
Published: BMJ Group, 2010
ISSN: 0022-2593
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View Full Text Source:Journal of Medical Genetics,Journal of Medical Genetics,BMJ Journals All Titles Opens in new Window
Journal:  Journal of Medical Genetics Source:BMJ Journals All Titles Opens in new Window
Collection:  BMJ Journals All Titles Opens in new Window
Coverage:
  • 1964~present; volume:1~present;issue:1~present
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