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Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes.
Flynn, Elizabeth K; Kamat, Aparna; Lach, Francis P; Donovan, Frank X; Kimble, Danielle C; Narisu, Narisu; Sanborn, Erica; Boulad, Farid; Davies, Stella M; Gillio, Alfred P; Harris, Richard E; MacMillan, Margaret L; Wagner, John E; Smogorzewska, Agata; Auerbach, Arleen D; Ostrander, Elaine A; Chandrasekharappa, Settara C.
Affiliation
  • Flynn EK; Cancer Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, 20892.
Hum Mutat ; 35(11): 1342-53, 2014 Nov.
Article in En | MEDLINE | ID: mdl-25168418
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Genomics / Fanconi Anemia Complementation Group Proteins / Fanconi Anemia Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2014 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Genomics / Fanconi Anemia Complementation Group Proteins / Fanconi Anemia Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2014 Document type: Article