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Screening and Testing: Genetics
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Author(s)/Faculty: Deborah Barbouth, MD, FACMG; Ana Morales, MS, CGC; Ricardo Villalba, MD; Lisa G.
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Shaffer, PhD; Bassem A. Bejjani, MD; Natasha Shur, MD; Dianne Abuelo, MD; Siobhan M. Dolan, MD, MPH
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Source: Pediatric Annals
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Type: Journal
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Number of Articles: 4
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Release Date: August 2009
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Expiration Date: August 31, 2012
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Cost: $25.00 / $105.00
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Credit Type: CME
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Number of Credit(s): 3.00
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Provider:
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OVERVIEW
The field of genetics has made considerable strides in the past few decades. As genetics continues to evolve, the diagnosis and care of those with genetic disorders improves. Healthcare providers are more quickly able to screen and identify, test, and diagnose patients with these conditions, thereby giving better opportunity for intervention services.
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- Genetic Syndromes: From Clinical Suspicion to Referral to Diagnosis
- Prenatal Genetic Testing
- Expanded Newborn Screening: An Update for Pediatricians
- Using Microarray-based Molecular Cytogenetic Methods to Identify Chromosome Abnormalities