Microdeletions – DiGeorge Syndrome (22q11.2 Deletion Syndrome)
- Oct 26, 2016 8:00 am
© 2016 By Keith S. Wexler, MBA, Maternal Fetal Medicine, Prenatal Diagnosis and Biotech/Life Sciences Consultant, GENASSIST, Inc. Paul Wexler, M.D., F.A.C.O.G., Medical Director, GENASSIST, Inc. Clinical Professor, Department of OB/GYN, University of Colorado Health Sciences Center Clinical Professor, Division of Genetics/Dept. of Pediatrics, Univ. of Colorado/The Children’s Hospital Background: Fetal DNA from the trophoblasts circulating in […]
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