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Volumn 31, Issue 3, 2004, Pages 621-625

Clinical consult: Developmental delay/fragile X syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BEHAVIOR THERAPY; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DIAGNOSTIC TEST; DIAGNOSTIC VALUE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; FRAGILE X SYNDROME; GENE MUTATION; GENETIC ANALYSIS; GENETIC COUNSELING; HAPPY PUPPET SYNDROME; HEREDITY; HUMAN; INHERITANCE; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; OCCUPATIONAL THERAPY; PHYSICAL EXAMINATION; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; RETT SYNDROME; SOTOS SYNDROME; SPEECH THERAPY; TREATMENT OUTCOME; TREATMENT PLANNING;

EID: 4344629379     PISSN: 00954543     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pop.2004.04.008     Document Type: Review
Times cited : (7)

References (12)
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  • 3
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  • 5
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  • 7
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    • Allingham-Hawkins D.J., Babul-Hirji R., Chitayat D., Holden J.J., Yang K.T., Lee C., et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study - preliminary data. Am J Med Genet. 83:(4):1999;322-325
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.