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Citations
Descartes M, Carroll AJ (2007). Cytogenetics. In RM Kliegman et al., eds., Nelson Textbook of Pediatrics, 18th ed., pp. 502–517. Philadelphia: Saunders Elsevier.
Cunningham FG, et al. (2010). Prenatal diagnosis and fetal therapy. In Williams Obstetrics, 23rd ed., pp. 287–311. New York: McGraw-Hill Medical.
Elias ER, et al. (2007). Chromosomal disorders: Abnormal number section of Genetics and dysmorphology. In WW Hay et al., eds., Current Pediatric Diagnosis and Treatment, 18th ed., pp. 1031–1032. New York: Lange Medical Books/McGraw-Hill.
Saitta SC, Zackai EH (2005). Specific chromosome disorders in newborns. In HW Taeusch et al., eds., Avery's Diseases of the Newborn, 8th ed., pp. 204–215. Philadelphia: Elsevier Saunders.
American College of Obstetricians and Gynecologists (2007, reaffirmed 2008). Screening for fetal chromosomal abnormalities. ACOG Practice Bulletin No. 77. Obstetrics and Gynecology, 109(1): 217–227.
Other Works Consulted
American Academy of Pediatrics, American Academy of Family Physicians, and American College of Physicians-American Society of Internal Medicine (2002). A consensus statement on health care transitions for young adults with special health care needs. Pediatrics, 110(6): 1304–1306.
Committee on Genetics, American Academy of Pediatrics (2001, reaffirmed 2007). Health supervision for children with Down syndrome. Pediatrics, 107(2): 442–449.
Driscoll DD, Gross SJ (2008). First trimester diagnosis and screening for fetal aneuploidy. Genetics in Medicine, 10(1): 73–75.
| By: | Healthwise Staff | Last Revised: February 10, 2010 |
| Medical Review: | Michael J. Sexton, MD - Pediatrics Siobhan M. Dolan, MD, MPH - Reproductive Genetics David Smith, MD - Family Medicine | |
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