Codon/geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (2)
- Morris, Michael Andréw (2)
- Neerman Arbez, Marguerite (2)
- Rossier, Colette (2)
- Abu-Libdeh, Bassam (1)
- Blouin, Jean-Louis (1)
- Bornholdt, D. (1)
- Bottani, Armand (1)
- Bouchardy, Isabelle (1)
- Chandal, D. (1)
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remove all| Title | Authors / Editors | Date | |
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Evolution of genes and genomes on the Drosophila phylogeny | Drosophila 12 Genomes Consortium | 2007 |
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Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family | Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw | 2003 |
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Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency | Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G. | 1999 |
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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations | Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos | 1999 |
