Imaging clues in the prenatal diagnosis of syndromes and aneuploidy

Author:

Estroff Judy A.

Publisher

Springer Science and Business Media LLC

Subject

Radiology Nuclear Medicine and imaging,Pediatrics, Perinatology, and Child Health

Reference48 articles.

1. Hennekam RC (2011) A newborn with unusual morphology: some practical aspects. Semin Fetal Neonatal Med 16:109–113

2. Stedman TL (2006) Stedman’s medical dictionary, 28th ed. Lippincott Williams & Wilkins, Philadelphia, 2199 pp

3. Estroff JA (2004) Prenatal diagnosis and imaging of genetic syndromes. Semin Roentgenol 39:323–335

4. Milunsky J, Milunsky A (2008) Genetic counseling in prenatal and perinatal medicine. In: Reece EA, Hobbins JC (eds) Clinical obstetrics: the fetus & mother. Wiley-Blackwell, Hoboken, NJ pp 318–335

5. Cicero S, Curcio P, Papageorghiou A et al (2001) Absence of nasal bone in fetuses with trisomy 21 at 11–14 weeks of gestation: an observational study. Lancet 358:1665–1667

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