Resource Center: genetic testing
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John B. Moeschler, MD, Michael Shevell, MD article published in the Pediatrics Journal
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AAFP 0
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In August 2002, Myriad launched an enhancement to the BRACAnalysis test to detect five common large rearrangements. The BRACAnalysis Rearrangement Test, or BART, launched in August 2006, is designed to detect large rearrangements beyond these five. For patients who meet the defined clinical criteria, BART will automatically be performed concurrently with the sequence analysis of Comprehensive BRACAnalysis®.
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Myriad Genetics Laboratory 0
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Fanconi anemia is an autosomal recessive disorder affecting all bone marrow elements and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes.
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Online Mendelian Inheritance in Men 0
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A journal article about the BRCA 2 Gene. The article details cloning, gene structure, mapping, gene function, role in DNA repair, and molecular genetics.
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Online Mendelian Inheritance in Men 0
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Dr. Duncan speaks about genetic testing and young people.
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University of Melbourne 0
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This article discusses both the well-known and the less common side effects of opioid use and the possible complications that can arise from this type of treatment.
Authors: Benyamin R, Trescot AM, Datta S, Buenaventura R, Adlaka R, Sehgal N, Glaser SE, Vallejo R
Issue: 11: S105-S120
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Pain Physician 2008: Opioids Special Issue 0
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This is a graphical version of the Sample Cancer Family History Questionnaire.
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Department of Health, New York 0
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Fanconi anemia (FA) is characterized by physical abnormalities, bone marrow failure, and increased risk of malignancy.
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GeneReviews 0
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This article provides information on the characteristics of Angelman syndrome, focusing on the genetic aspects such as genetic testing and genetic counseling.
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University of Washington 0
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This article provides information on the characteristics of Beckwith-Wiedemann Syndrome, focusing on the genetic aspects such as genetic testing and counseling.
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University of Washington 0
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