[FROM GENETICS OF FRAGILE X SYNDROME TO DEVELOPMENT OF TARGETED AND PERSONALIZED DRUG THERAPY].

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Last Posted: Sep 06, 2018

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• [FROM GENETICS OF FRAGILE X SYNDROME TO DEVELOPMENT OF TARGETED AND PERSONALIZED DRUG THERAPY].
  Gabis Lidia V et al. Harefuah 2018 Aug 157(8) 529-533
• Family History and Cancer
  CDC Division of Cancer Control and Prevention, 2018
• Know Your Body. Know Your Family History.
  Sun Hee Rim et al, CDC Blog, August 2018
• Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana.
  Dennis-Antwi Jemima A et al. Journal of genetic counseling 2018 Sep
• The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
  Li Meng et al. Journal of genetic counseling 2018 Sep
• Use of Electronic Health Record Integration for Down Syndrome Guidelines.
  Santoro Stephanie L et al. Pediatrics 2018 Sep 142(3)
• A survey study with assessment of esophageal screening and genetic counseling in patients with Howel-Evans syndrome.
  Jenkins Lauren E et al. Dermatology online journal 2018 Jun 24(6)
• Cancer Screening 
  Recommendations for individual patients vary according to their level of risk, Jackson Labs, clinician education
• Consumer Genetic Testing Will Change Your Life. In Fact, It Probably Already Has.
  E Matloff, Forbes, August 24, 2018
• Early genetic counseling and detection of CDH1 mutation in asymptomatic carriers improves survival in hereditary diffuse gastric cancer.
  Moslim Maitham A et al. Surgery 2018 Aug

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