Novel inactivating mutations of FANCC in Brazilian patients with Fanconi anemia.

Human mutation

Volumn 27, Issue 2, 2006, Pages 214-

  Yates, Jane ^a   Keeble, Winifred ^a   Pals, Gerard ^a   Ameziane, Najim ^a   van Spaendonk, Rosalina ^a   Olson, Susan ^a   Akkari, Yassmine ^a   Pasquini, Ricardo ^a   Bagby, Grover ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FANCONI ANEMIA GROUP C PROTEIN;

ARTICLE; BONE MARROW CELL; BRAZIL; CHILD; CYTOLOGY; EXON; FEMALE; GENE DELETION; GENETIC COMPLEMENTATION; GENETICS; HUMAN; MUTATION; NUCLEOTIDE SEQUENCE; RNA SPLICING;

BONE MARROW CELLS; BRAZIL; CHILD; DNA MUTATIONAL ANALYSIS; EXONS; FANCONI ANEMIA COMPLEMENTATION GROUP C PROTEIN; FEMALE; GENE DELETION; GENETIC COMPLEMENTATION TEST; HUMANS; MUTATION; RNA SPLICING;

EID: 33745952197     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9402     Document Type: Article

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