Author/Creator: El‐Maarri, O. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator El‐Maarri, O.

1. Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA. (12th September 2013)

Authors:: Pezeshkpoor, B.; Zimmer, N.; Marquardt, N.; Nanda, I.; Haaf, T.; Budde, U.; Oldenburg, J.; El‐Maarri, O.
Journal:: Journal of thrombosis and haemostasis
Issue:: Volume 11:Number 9(2013:Sep.)
Page Start:: 1679
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Evidence of pathogenicity of a mutation in 3′ untranslated region causing mild haemophilia A. (24th May 2016)

Authors:: Pezeshkpoor, B.; Berkemeier, A‐ C.; Czogalla, K. J.; Oldenburg, J.; El‐Maarri, O.
Journal:: Haemophilia
Issue:: Volume 22:Number 4(2016:Jul.)
Page Start:: 598
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Genetic testing in bleeding disorders. (May 2014)

Authors:: de Brasi, C.; El‐Maarri, O.; Perry, D. J.; Oldenburg, J.; Pezeshkpoor, B.; Goodeve, A.
Journal:: Haemophilia
Issue:: Volume 20(2014)Supplement 4
Page Start:: 54
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Novel characterization of a breakpoint in F8: an individualized approach to gene analysis when PCR and MLPA results contradict. (27th January 2015)

Authors:: Pezeshkpoor, B.; Theophilus, B. D. M.; Guilliatt, A. M.; Oldenburg, J.; Williams, M. D.; El‐Maarri, O.
Journal:: Haemophilia
Issue:: Volume 21:Number 3(2015:May)
Page Start:: 392
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗