Introns/ geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (1)
- Attanasio, Catia (1)
- David, Armelle (1)
- Krieg, T. (1)
- Marneros, A. G. (1)
- Mehenni, H. (1)
- Neerman Arbez, Marguerite (1)
- Olsen, B. R. (1)
- Reichenberger, E. (1)
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remove all| Title | Authors / Editors | Date | |
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Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA) | Attanasio, Catia; David, Armelle; Neerman Arbez, Marguerite | 2003 |
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Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome | Marneros, A. G.; Mehenni, H.; Reichenberger, E.; Antonarakis, Stylianos; ... Olsen, B. R. | 2001 |
