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- W2082510117 abstract "New molecular research has provided strong evidence for different forms of the fragile X mutation. These findings suggest the need to develop a more standardized and sensitive method for determining neurobehavioral effects of the fragile X gene(s), particularly for molecular studies of patients who do not have obvious mental retardation. This report describes a brief screening questionnaire designed to increase the detection of neurobehavioral dysfunction in individuals from fragile X families who are included in new molecular studies. Improved detection of the affected state in fragile X syndrome will allow more valid clinical data to be correlated with the important molecular information currently being collected." @default.
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- W2082510117 date "1992-04-15" @default.
- W2082510117 modified "2023-10-16" @default.
- W2082510117 title "Brief screening questionnaire for determining affected state in fragile X Syndrome: A consensus recommendation" @default.
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- W2082510117 doi "https://doi.org/10.1002/ajmg.1320430109" @default.
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