Using a parent survey to advance knowledge about the nature and consequences of fragile X syndrome

American Journal on Intellectual and Developmental Disabilities

Volumn 115, Issue 6, 2010, Pages 447-460

  Bailey Jr , Donald B ^a   Raspa, Melissa ^a   Olmsted, Murrey G ^a  

^a RTI INTERNATIONAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; COST BENEFIT ANALYSIS; DISABILITY; ECONOMICS; FRAGILE X SYNDROME; GENETICS; HEALTH SURVEY; HUMAN; MENTAL DEFICIENCY; METHODOLOGY; PARENT; PATHOPHYSIOLOGY; UNITED STATES;

ADULT; CHILD; COST-BENEFIT ANALYSIS; DISABILITY EVALUATION; FRAGILE X SYNDROME; HEALTH SURVEYS; HUMANS; MENTAL RETARDATION; PARENTS; UNITED STATES;

EID: 79952111698     PISSN: 19447558     EISSN: None     Source Type: Journal    
DOI: 10.1352/1944-7558-115.6.447     Document Type: Review

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