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BMC BIOINFORMATICS, ISSN 1471-2105, 06/2019, Volume 20, Issue 1, pp. 363 - 13
Journal Article
Journal Article
Haemophilia, ISSN 1351-8216, 05/2019, Volume 25, Issue 3, pp. 475 - 483
Introduction Only two large duplications of F9 causing haemophilia B (HB) have been reported. Aim To analyse the pathogenic mechanisms of large F9... 
genomic rearrangement | promoter competition | haemophilia B | large duplication | somatic and germline mosaicism | MECHANISM | TANDEM | F9 MESSENGER-RNA | UNUSUAL EXPRESSION | REARRANGEMENTS | GENOME | BREAKPOINTS | GENE | ARCHITECTURE | TRANSCRIPTIONAL INTERFERENCE | HEMATOLOGY | Genomics | Analysis | Hemophilia | Breakpoints | Transcription | Pedigree | Mitosis | Mosaicism | Genomes | Gene mapping
Journal Article
Journal Article
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 11/2013, Volume 1, Issue 4, pp. 238 - 245
Hemophilia B (HB) is caused by mutations in the human gene F9. The mutation type plays a pivotal role in genetic counseling and prediction of inhibitor... 
mutation database | F9 gene | hemophilia B | Genetic counseling | Hemophilia | Mutation | Accessibility | Peptides | Internet resources | Nomenclature | Amino acids | Genomes | Gene expression | Disease control | Genetic screening | Data bases | Proteins | Genotype & phenotype | Researchers | Inhibitors | Etiology | Predictions | Genetic counselling | Original
Journal Article
Journal Article