Prenatal detection of 22q11.2 deletion syndrome and congenital heart disease.
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| Title: | Prenatal detection of 22q11.2 deletion syndrome and congenital heart disease. |
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| Authors: | Freud LR; The Hospital for Sick Children, University of Toronto, Department of Paediatrics, Division of Cardiology, 555 University Avenue, Toronto, ON M5G 1X8, Canada. Electronic address: lindsay.freud@sickkids.ca., Wapner R; NewYork Presbyterian Hospital, Columbia University Irving Medical Center, New York City, NY., McDonald-McGinn DM; Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Department of Pediatrics, Division of Human Genetic, Philadelphia, PA. |
| Source: | American journal of obstetrics and gynecology [Am J Obstet Gynecol] 2024 Apr; Vol. 230 (4), pp. e50. Date of Electronic Publication: 2023 Nov 11. |
| Publication Type: | Letter; Comment |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 0370476 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6868 (Electronic) Linking ISSN: 00029378 NLM ISO Abbreviation: Am J Obstet Gynecol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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