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Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.

• Authors : Gille, Johan J. P.; Floor, Karijn; Kerkhoven, Lianne

• Source: Anemia (20901267); 2012, p1-13, 13p, 4 Charts

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Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis.

• Authors : Oostra, Anneke B.; Nieuwint, Aggie W. M.; Joenje, Hans

• Source: Anemia (20901267); 2012, p1-9, 9p, 1 Diagram, 1 Chart, 1 Graph

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Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing.

• Authors : Ameziane, Najim; Sie, Daoud; Dentro, Stefan

• Source: Anemia (20901267); 2012, p1-7, 7p, 2 Diagrams, 3 Charts, 2 Graphs

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Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome.

• Authors : van der Lelij, Petra; Oostra, Anneke B.; Rooimans, Martin A.

• Source: Anemia (20901267); 2010, p1-7, 7p, 1 Chart, 3 Graphs

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No evidence for FANCF gene silencing in head-and-neck squamous cell carcinomas.

• Authors : Ameziane, Najim; Fei Chen; Leemans, C. René

Subjects: LETTERS to the editor; CANCER patients

• Source: Cellular Oncology; Jan2009, Vol. 31 Issue 1, p53-56, 4p, 1 Black and White Photograph

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Genetic subtyping of Fanconi anemia by comprehensive mutation screening.

• Authors : Ameziane, Najim; Errami, Abdellatif; Léveillé, France

• Source: Human Mutation; Jan2008, Vol. 29 Issue 1, p159-166, 8p

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Identification of the Fanconi anemia complementation group I gene, FANCI.

• Authors : Dorsman, Josephine C.; Levitus, Marieke; Rockx, Davy

Subjects: DATA mining; DATABASE searching; FANCONI'S anemia

• Source: Cellular Oncology; May2007, Vol. 29 Issue 3, p211-218, 8p, 1 Diagram, 2 Charts, 3 Graphs

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The Fanconi anemia pathway of genomic maintenance.

• Authors : Levitus, Marieke; Joenje, Hans; de Winter, Johan P.

Subjects: FANCONI'S anemia; ANEMIA; GENOMICS

• Source: Cellular Oncology; Jan2006, Vol. 28 Issue 1/2, p3-29, 27p, 7 Diagrams, 1 Chart

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Exon 6 skipping in the fanconi anemia C gene associated with a nonsense/missense mutation (775C→T) in exon 5: The first example of a nonsense mutation in one exon causing skipping of another downstream.

• Authors : Lo Ten Foe, Jerome R.; Kruyt, Frank A.E.; Zweekhorst, Marjolein B.M.

• Source: Human Mutation; 1998 Supplement, Vol. 11, pS25-S27, 3p

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Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia c gene, FAC.

• Authors : Lo Ten Foe, Jerome R.; Rooimans, Martin A.; Joenje, Hans

• Source: Human Mutation; 1996, Vol. 7 Issue 3, p264-265, 2p

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