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Volumn 15, Issue 1, 2007, Pages 127-130

Changing rates of genetic subtypes of Prader-Willi syndrome in the UK

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11Q; CHROMOSOME 13Q; CHROMOSOME 15; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL ARTICLE; CONCEPTION; GENE DELETION; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INFANT; MATERNAL AGE; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; RISK ASSESSMENT; UNIPARENTAL DISOMY; UNITED KINGDOM;

EID: 33845515071     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201716     Document Type: Article
Times cited : (47)

References (13)
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  • 3
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  • 5
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  • 8
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    • Genomic imprinting as a cause of disease
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.