PREMIER Biosoft logo  

Download Flyer
MLPA® Designer is a comprehensive tool co-developed with MRC-Holland to design highly specific oligos for MLPA® assays.
Home >> Products >> MLPA® Designer >> Citations & Reviews
PREMIER Biosoft Facebook link PREMIER Biosoft Twitter link
MLPA® Designer

Citations and Reviews

Author and Details
Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing Morinière, V., Dahan, K., Hilbert, P., Lison, M., Lebbah, S., Topa, A., Bole-Feysot, Christine., Pruvost, Solenn., Nitschke, Patrick., Plaisier, Emmanuelle., Knebelmann, Bertrand., Macher, Marie-Alice., Noel, Laure-Hélène., Gubler, Marie-Claire., Antignac, Corinne., Heidet, Laurence. (2014)
J Am Soc Nephrol, 25(12), 2740–2751.

Germ-line deletion in DICER1 revealed by a novel MLPA assay using synthetic oligonucleotides

Sabbaghian, N., Srivastava, A., Hamel, N., Plourde, F., Gajtko-Metera, M., Niedziela, M., Foulkes, W.D. (2014). Eur J Hum Genet, 22(4), 564-7.


Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group

Gratias, E. J., Jennings, L. J., Anderson, J. R., Dome, J. S., Grundy, P., & Perlman, E. J. (2013). Cancer, 119(21), 3887-3894.


A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome

Holm, I., Monclair, T., Lundar, T., Stadheim, B., Prescott, T. E., & Eiklid, K. L. (2013). Gene, 518(2), 457-460.


Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., ... & Kehrer‐Sawatzki, H. (2012). Human mutation, 33(11), 1599-1609.


BeeDoctor, a Versatile MLPA-Based Diagnostic Tool for Screening Bee Viruses

De Smet, L., Ravoet, J., de Miranda, J. R., Wenseleers, T., Mueller, M. Y., Moritz, R. F., & De Graaf, D. C. (2012). PloS one, 7(10), e47953.


Two New Rapid SNP-Typing Methods for Classifying Mycobacterium tuberculosis Complex into the Main Phylogenetic Lineages

Stucki, D., Malla, B., Hostettler, S., Huna, T., Feldmann, J., Yeboah-Manu, D., ... & Gagneux, S. (2012). PLoS One, 7(7), e41253.


Four unrelated patients with lubs X-linked mental retardation syndrome and different Xq28 duplications

Bartsch, O., Gebauer, K., Lechno, S., Van Esch, H., Froyen, G., Bonin, M., ... & Haaf, T. (2010). American Journal of Medical Genetics Part A, 152(2), 305-312.

Note: MLPA Designer, the lite version of AlleleID, includes the MLPA module of AlleleID.
Copyright ©1994- PREMIER Biosoft. All rights reserved.