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Volumn 36, Issue 3, 1996, Pages 539-542

Genomic imprinting and chromosomal localization of the human MEST gene

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARCINOGENESIS; CHROMOSOME 7Q; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION REGULATION; GENE LOCATION; GENE SEQUENCE; HUMAN; HYDATIDIFORM MOLE; MESODERM; MOUSE; NONHUMAN; NORTHERN BLOTTING; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TERATOMA; TISSUE SPECIFICITY;

EID: 0030587572     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0502     Document Type: Article
Times cited : (41)

References (15)
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  • 8
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    • Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes
    • 8. Nicholls, R. D. (1993). Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes. Curr. Opin. Genet. Dev. 3: 445-456.
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    • Nicholls, R.D.1
  • 10
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    • Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome
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  • 12
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    • Zhang, Y.1    Shields, T.2    Crenshaw, T.3    Hao, Y.4    Moulton, T.5    Tycko, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.