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Iranian Journal of Public Health، جلد ۴۷، شماره ۷، صفحات ۱۰۵۸-۱۰۶۰
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عنوان انگلیسی Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome
چکیده انگلیسی مقاله No Abstract 1. Moeschler JB, Shevell M (2014). Comprehensive evaluation of the child with intellectual disability or global developmental delays. Pediatrics, 134(3):e903-18. 2. Soltani S, Khosravi B, Salehiniya H (2015). Prevalence of intellectual disability in Iran: Toward a new conceptual framework in data collection. J Res Med Sci, 20(7):714-5. 3. Soltani Banavandi MJ, Kahrizi K, Behjati F et al (2012). Investigation of Genetic Causes of Intellectual Disability in Kerman Province, South East of Iran. Iran Red Crescent Med J, 14(2):79-85. 4. Centers for Disease Control and Prevention (CDC) (2002). Delayed diagnosis of fragile X syndrome--United States, 1990-1999. MMWR Morb Mortal Wkly Rep, 51(33):740-742. 5. Bailey DB Jr, Raspa M, Bishop E, Holiday D (2009). No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey. Pediatrics, 124(2):527-33. 6. Hersh JH, Saul RA, Committee on Genetics (2011). Health Supervision for Children With Fragile X Syndrome. Pediatrics , 127(5):994-1006. 7. Levenson D (2014). Facial analysis technology aids diagnoses of genetic disorders: applications narrow down potential genetic syndromes by matching facial phenotypes to distinct set of possible genetic conditions. Am J Med Genet A, 164A(10):vii-viii.
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نویسندگان مقاله | Reza JAFARZADEH ESFEHANI
Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran Stem Cell and Regenerative Medicine Research Group, Academic Center for Education, Culture and Research (ACECR), Khorasan Razavi Branch, Mashhad, Iran


| Mahtab DASTPAK
Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran


| Mohammad Reza MIRINEZHAD
Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran


| Ariane SADR-NABAVI


نشانی اینترنتی http://ijph.tums.ac.ir/index.php/ijph/article/view/14062
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زبان مقاله منتشر شده en
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نوع مقاله منتشر شده Letter to the Editor
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