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Volumn 111, Issue 4, 2002, Pages 440-442

Estimate of prevalence of proximal 15q duplication syndrome [1]

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 15Q; CHROMOSOME DUPLICATION; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FEMALE; FRAGILE X SYNDROME; GENE AMPLIFICATION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HAPPY PUPPET SYNDROME; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; CHROMOSOME 15; GENE DUPLICATION; GENETICS; INFANT; MULTIPLE MALFORMATION SYNDROME;

EID: 0036707805     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10419     Document Type: Letter
Times cited : (14)

References (9)
  • 6
    • 0034532203 scopus 로고    scopus 로고
    • Characteristics of two cases with dup(15)(q11.2-q12): One of maternal and one of paternal origin
    • (2000) Genet Med , vol.2 , pp. 131-135
    • Mao, R.1    Jalal, S.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.