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Volumn 77, Issue 4, 2010, Pages 447-449

Clinical and behavioural profile of a rare variant of klinefelter syndrome-48, XXXY

Author keywords

FISH; Gene dosage effects; Karyotype; Klinefelter; Mosaicism

Indexed keywords

ARTICLE; BEHAVIOR CHANGE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CLINICAL EXAMINATION; CLINICAL FEATURE; CLINODACTYLY; COGNITION; CRYPTORCHISM; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPOGONADISM; INCIDENCE; INDIA; KLINEFELTER SYNDROME; MALE; MENTAL DEFICIENCY; PSYCHOLOGIC ASSESSMENT; SCHOOL CHILD; SCREENING TEST; X CHROMOSOME; ANEUPLOIDY; DEVELOPMENTAL DISORDER; GENETICS;

EID: 77955946861     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-009-0288-6     Document Type: Article
Times cited : (4)

References (10)
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  • 3
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  • 4
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    • Cytogenetic analysis of a boy with XXXY syndrome-origin of the X chromosome
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  • 5
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.