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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2010, Volume 107, Issue 5, pp. 1864 - 1869
Journal Article
HAMOSTASEOLOGIE, ISSN 0720-9355, 08/2018, Volume 38, Issue 3, pp. 158 - 165
Molecular testing of congenital coagulation and platelet disorders offers confirmation of clinical diagnoses, supports genetic counselling, and enables... 
FACTOR-X DEFICIENCY | FACTOR-VII DEFICIENCY | IDENTIFICATION | BRCA2 | MOLECULAR ANALYSIS | LR-PCR | FACTOR-XII GENE | MUTATION | THROMBOCYTOPENIA | NGS | high throughput sequencing | APPARENT HOMOZYGOSITY | MISDIAGNOSIS | HEMATOLOGY | congenital coagulation and platelet disorders
Journal Article
Journal of Gastroenterology and Hepatology, ISSN 0815-9319, 10/2019, Volume 34, Issue 10, pp. 1851 - 1859
Journal Article
Cell Stem Cell, ISSN 1934-5909, 08/2015, Volume 17, Issue 2, pp. 213 - 220
Hemophilia A is an X-linked genetic disorder caused by mutations in the gene, which encodes the blood coagulation factor VIII. Almost half of all severe... 
CRISPR/CAS9 | SPECIFICITY | TALENS | HUMAN-CELLS | OFF-TARGET CLEAVAGE | NUCLEASES | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Factor VII - genetics | Animals | Base Sequence | Humans | Molecular Sequence Data | Clone Cells | Hemophilia A - genetics | Mice | HeLa Cells | CRISPR-Cas Systems - genetics | Chromosome Inversion - genetics | Induced Pluripotent Stem Cells - metabolism
Journal Article
BMC BIOINFORMATICS, ISSN 1471-2105, 06/2019, Volume 20, Issue 1, pp. 363 - 13
Journal Article
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 02/2008, Volume 99, Issue 2, pp. 388 - 395
Journal Article
Journal of Controlled Release, ISSN 0168-3659, 06/2016, Volume 232, pp. 143 - 151
Journal Article