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851P Frequency and clinical significance of homologous recombination deficiency gene mutations in non-cutaneous melanoma.

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Title: 851P Frequency and clinical significance of homologous recombination deficiency gene mutations in non-cutaneous melanoma.
Authors: Yang, Y.1 (AUTHOR), Lian, B.1 (AUTHOR), Si, L.1 (AUTHOR), Chi, Z.1 (AUTHOR), Sheng, X.1 (AUTHOR), Kong, Y.1 (AUTHOR), Cui, C-L.1 (AUTHOR), Guo, J.1 (AUTHOR)
Source: Annals of Oncology. 2022 Supplement 7, Vol. 33, pS939-S939. 1p.
Database: Academic Search Ultimate
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  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 159077768
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: 851P Frequency and clinical significance of homologous recombination deficiency gene mutations in non-cutaneous melanoma.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Oncology%22">Annals of Oncology</searchLink>. 2022 Supplement 7, Vol. 33, pS939-S939. 1p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=159077768
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1016/j.annonc.2022.07.977
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      – Code: eng
        Text: English
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        PageCount: 1
        StartPage: S939
    Titles:
      – TitleFull: 851P Frequency and clinical significance of homologous recombination deficiency gene mutations in non-cutaneous melanoma.
        Type: main
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            NameFull: Yang, Y.
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            NameFull: Lian, B.
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            NameFull: Si, L.
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            NameFull: Chi, Z.
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            NameFull: Sheng, X.
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            NameFull: Kong, Y.
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            NameFull: Cui, C-L.
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            NameFull: Guo, J.
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            – D: 02
              M: 09
              Text: 2022 Supplement 7
              Type: published
              Y: 2022
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              Value: 33
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            – TitleFull: Annals of Oncology
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