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Volumn 28, Issue 3, 2001, Pages 294-296

Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17Q; GENE MUTATION; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MITOSIS; NEUROFIBROMA; PRIORITY JOURNAL;

EID: 0034938366     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/90148     Document Type: Article
Times cited : (59)

References (25)
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  • 4
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    • (1997) Biochem. Biophys. Res. Commun. , vol.234 , pp. 346-350
    • Daschner, K.1
  • 5
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    • Confirmation of a double-hit model for the NF1 gene in benign neurofibromas
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 512-519
    • Serra, E.1
  • 10
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    • Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations
    • (2001) Hum. Genet. , vol.108 , pp. 416-429
    • Serra, E.1
  • 12
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    • Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
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    • Cavenee, W.K.1
  • 16
    • 0001795270 scopus 로고    scopus 로고
    • Double mitotic recombination at common breakpoint intervals leading to interstitial isodisomy and LOH
    • (1998) Am. J. Hum. Genet. , vol.63
    • Stephens, K.1
  • 17
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  • 18
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    • Gupta, P.K.1
  • 21
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    • Cancer predisposition caused by elevated mitotic recombination in bloom mice
    • (2000) Nature Genet. , vol.26 , pp. 424-429
    • Luo, G.1
  • 24
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    • Mutation affecting mRNA splicing are the most common molecular defects in patients with neurobiromatosis type 1
    • (2000) Hum. Mol. Genet. , vol.9 , pp. 237-247
    • Ars, E.1
  • 25
    • 0031029826 scopus 로고    scopus 로고
    • Down syndrome: Characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.