کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2675981 | 1141827 | 2008 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Assessment of FMR1 Gene Mutation at-Risk Status in Young Children
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
پریناتولوژی (پزشکی مادر و جنین)، طب اطفال و بهداشت کودک
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Assessment of FMR1 Gene Mutation at-Risk Status in Young Children Assessment of FMR1 Gene Mutation at-Risk Status in Young Children](/preview/png/2675981.png)
چکیده انگلیسی
Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene, is the most commonly inherited cause of developmental disability. Fragile X syndrome occurs relatively equally in all racial and ethnic groups and is one of the few disorders affecting child behavior for which the exact gene is identified. Furthermore, from infancy, both males and females with this syndrome are predisposed for manifesting characteristic cognitive, emotional, and behavioral challenges. The purpose of this article is to illuminate the multisystemic and multifaceted phenotype of the FMR1 gene mutation by means of the parent response Biopsychosocial Screening Inventory for Fragile X, for which preliminary studies show promise.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Newborn and Infant Nursing Reviews - Volume 8, Issue 1, March 2008, Pages 10–17
Journal: Newborn and Infant Nursing Reviews - Volume 8, Issue 1, March 2008, Pages 10–17
نویسندگان
Vanessa Althea Thomas Johnson,