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Volumn 103, Issue 1, 2004, Pages 366-

Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE MEGAKARYOCYTIC LEUKEMIA; AMINO TERMINAL SEQUENCE; CASE REPORT; DNA EXTRACTION; DOWN SYNDROME; EXON; FEMALE; FETUS; GATA1 GENE; GENE; GENE MUTATION; GENE SEQUENCE; HUMAN; LETTER; MONOZYGOTIC TWINS; MYELOPROLIFERATIVE DISORDER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STOP CODON; TRISOMY 21;

EID: 0346966816     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2003-09-3219     Document Type: Letter
Times cited : (50)

References (9)
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  • 2
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    • (2003) Blood , vol.101 , pp. 4301-4304
    • Hitzler, J.K.1    Cheung, J.2    Li, Y.3
  • 4
    • 0042243593 scopus 로고    scopus 로고
    • Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
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  • 5
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    • Groet, J.1    McElwaine, S.2    Spinelli, M.3
  • 6
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  • 7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.