Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome von Albers, Cornelis A, Ouwehand, Willem H, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross N W, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita

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A systematic genome-wide analysis of zebrafish protein-coding gene function von Kettleborough, Ross N. W., Busch-Nentwich, Elisabeth M., Harvey, Steven A., Dooley, Christopher M., de Bruijn, Ewart, van Eeden, Freek, Sealy, Ian, White, Richard J., Herd, Colin, Nijman, Isaac J., Fényes, Fruzsina, Mehroke, Selina, Scahill, Catherine, Gibbons, Richard, Wali, Neha, Carruthers, Samantha, Hall, Amanda, Yen, Jennifer, Cuppen, Edwin, Stemple, Derek L.

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Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution von McConnell, Sean C., Hernandez, Kyle M., Wcisel, Dustin J., Kettleborough, Ross N., Stemple, Derek L., Yoder, Jeffrey A., Andrade, Jorge, de Jong, Jill L. O.

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Efficient identification of CRISPR/Cas9-induced insertions/deletions by direct germline screening in zebrafish von Brocal, Isabel, White, Richard J, Dooley, Christopher M, Carruthers, Samantha N, Clark, Richard, Hall, Amanda, Busch-Nentwich, Elisabeth M, Stemple, Derek L, Kettleborough, Ross N W

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Multi-allelic phenotyping – A systematic approach for the simultaneous analysis of multiple induced mutations von Dooley, Christopher M., Scahill, Catherine, Fényes, Fruzsina, Kettleborough, Ross N.W., Stemple, Derek L., Busch-Nentwich, Elisabeth M.

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Essential and overlapping roles for laminin α chains in notochord and blood vessel formation von Pollard, Steven M., Parsons, Michael J., Kamei, Makoto, Kettleborough, Ross N.W., Thomas, Kevin A., Pham, Van N., Bae, Moon-Kyoung, Scott, Annabelle, Weinstein, Brant M., Stemple, Derek L.

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Exome sequencing identifies NBEAL2 as the causative genefor gray platelet syndrome von Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross N W, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H

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Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome von Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H

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