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Volumn 34, Issue 11, 1997, Pages 917-923

Prader-Willi syndrome

Author keywords

Imprinting; Prader Willi syndrome; Proximal 15q; Uniparental disomy

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CHROMOSOME 15Q; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; FACIES; GENOME IMPRINTING; GROWTH RETARDATION; HUMAN; HYPOGONADISM; HYPOTHALAMUS FUNCTION DISORDER; INFANTILE HYPOTONIA; INTERSTITIAL CHROMOSOME DELETION; MENTAL DEFICIENCY; MORBIDITY; MORTALITY; OBESITY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RECURRENCE RISK; SHORT STATURE; UNIPARENTAL DISOMY;

EID: 0030726998     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.11.917     Document Type: Article
Times cited : (407)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.