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Volumn 68, Issue 1, 2001, Pages 247-253

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME 14; CHROMOSOME 15; CHROMOSOME 6; CHROMOSOME 7Q; DEVELOPMENT; GENE CLUSTER; GROWTH REGULATION; HUMAN; INHERITANCE; MOTHER; PARENT; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY; ZYGOTE;

EID: 0035168178     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/316937     Document Type: Article
Times cited : (111)

References (43)
  • 9
    • 0018939994 scopus 로고
    • A new genetic concept: Uniparental disomy and its potential effect, isodisomy
    • (1980) Am J Med Genet , vol.6 , pp. 137-143
    • Engel, E.1
  • 27
    • 0022568782 scopus 로고
    • X-linked short stature with skin pigmentation: Evidence for heterogeneity of the Russell-Silver syndrome
    • (1986) Clin Genet , vol.29 , pp. 151-156
    • Partington, M.W.1
  • 32
    • 0000771975 scopus 로고
    • A syndrome of "Intra-uterine" dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples)
    • (1954) Proc R Soc Med , vol.47 , pp. 1040-1044
    • Russell, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.