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Volumn 23, Issue 4, 2000, Pages 715-724

Genomic imprinting: Genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRANSCRIPTION FACTOR; UBE3A PROTEIN; UBIQUITIN PROTEIN LIGASE; UNCLASSIFIED DRUG;

EID: 0034431527     PISSN: 14154757     EISSN: None     Source Type: Journal    
DOI: 10.1590/S1415-47572000000400004     Document Type: Review
Times cited : (5)

References (24)
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  • 9
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    • Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/ Angelman syndromes
    • Buiting, K., Grob, S., Ji, Y., Senger, G., Nicholls, R.D. and Horsthemke, B. (1998a). Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/ Angelman syndromes. Cytogenetic. Cell Genet. 81: 247-253.
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  • 12
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    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 777-784
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  • 13
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    • Hypopigmentation: A common feature of Prader-Labhart-Willi syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.